Methods for the modulation of il-13

ABSTRACT

The present invention is drawn to methods for modulating IL-13 expression and/or activity in a mammal comprising administering an effective amount of an agent which modulates the expression and/or activity of IL-9.

CROSS-REFERENCE TO RELATED APPLICATIONS

[0001] This invention claims the benefit of U.S. provisional application 60/297,190, filed Jun. 8, 2001, and is a continuation-in-part of U.S. patent application Ser. No. 09/848,585, filed May 4, 2001, which is a continuation of U.S. patent application Ser. No. 09/325,571 filed on Jun. 6, 1999, now U.S. Pat. No. 6,261,559, which are herein incorporated by reference in their entirety.

FIELD OF THE INVENTION

[0002] This invention relates to modulation of the IL-13 expression and activity in a mammal though modulation of IL-9 expression and activity.

BACKGROUND OF THE INVENTION

[0003] Interleukin-13 (IL-13) is a cytokine expressed in inflammatory immune responses that are controlled by Th2-type T lymphocytes (Minty et al. (1993) Nature 362, 248-250; McKenzie et al. (1993) Proc. Natl. Acad. Sci. USA 90, 3735-3739). Recently it has been suggested that IL-13 plays a central role in the pathogenesis of asthma (Wills-Karp et al. (1998) Science 282, 2258-2261; Grunig et al. (1998) Science 282, 2261-2263) and transgenic expression of IL-13 in the lung produced an asthmatic like response (Zhu et al. (1999) J. Clin. Invest. 103, 779-788). IL-13 expression is also found to be elevated in asthma patients (Walker et al. (1992) Am. Rev. Respir. Dis. 146, 109-115; Humbert et al. (1997) J. Allergy Clin. Immunol. 99, 657-665; Huang (1995) J. Immunol. 155, 2688-2694) and asthma has been genetically linked to chromosome 5q, a region that contains both the IL-13 and the IL-9 genes (Marsh et al. (1996) Science 264, 1152-1156).

[0004] Based on the data presented in the patent applications listed above, there is substantial support for the role of the cytokine IL-9 in the pathogenesis of asthma. First, applicants demonstrate linkage homology between humans and mice, suggesting the same gene is responsible for producing biologic variability in response to antigen in both species. Second, differences in expression of the murine IL-9 candidate gene are associated with biologic variability in bronchial responsiveness. In particular, reduced expression of IL-9 is associated with a lower baseline bronchial response in B6 mice. Third, recent evidence for linkage disequilibrium in data from humans suggests IL-9 may be associated with atopy and bronchial hyperresponsiveness consistent with a role for this gene in both species (Doull et al. (1996) Am. J. Respir. Crit. Care Med. 153, 1280-1284). Moreover, applicants have demonstrated that a genetic alteration in the human gene appears to be associated with loss of cytokine function and lower IgE levels. Fourth, the pleiotropic functions of this cytokine and its receptor in the allergic immune response strongly support a role for the IL-9 pathway in the complex pathogenesis of asthma. Fifth, in humans, biologic variability in the IL-9 receptor also appears to be associated with atopic allergy and asthma. Finally, despite the inherited loss of IL-9 receptor function, these individuals appear to be otherwise healthy. Thus, nature has demonstrated in atopic individuals that the therapeutic down-regulation of IL-9 and IL-9 receptor genes or genes activated by IL-9 and its receptor is likely to be safe and useful for the treatment of asthma.

[0005] In some infectious diseases it has recently been suggested that elevated levels of IL-13 may contribute to the pathogenesis of the disease. For example, in patients with tuberculosis it has been demonstrated that there is a very large relative increase in IL-4 and IL-13 expression, that correlates with lung damage and indicates that a T helper-2 (Th2) component in the response to M. tuberculosis may undermine the efficacy of immunity and contribute to immunopathology (Rook et al. (2001) Curr. Opin. Pulm. Med. 7, 116-123). In addition, in patients with dengue hemorrhagic fever it has been suggested that high levels of IL-13 may contribute to the shift from a Th1 to Th2 type response and thus to the pathogenesis of the disease (Mustafa et al. (2001) FEMS Immunol. Med. Microbiol. 30, 229-233).

[0006] High levels of IL-13 have also associated with diseases that are characterized by fibrosis (Oriente et al. (2000) J. Pharmacol. Exp. Ther. 292, 988-994), for example Hodgkin's disease (Ohshima et al. (2001) Histopathology 38, 368-375).

[0007] IL-13 has also been shown to be capable of up-regulating the enzyme 15-lipoxygnase and the down-regulation of its isozyme 5-lipoxygenase (Nassar et al. (1994) J. Biol. Chem. 269, 27631-27634; Spanbroek et al. (2001) Proc. Natl. Acad. Sci. USA 98, 5152-5157). The net effect appears to be the down-regulation of a Th1 mediated inflammatory response.

[0008] It has previously been shown that IL-9 is important in asthma and other inflammatory diseases. The present invention is based, in part, upon the discovery described herein that control IL-9 levels can be utilized to control IL-13 levels in inflammatory diseases such as asthma.

SUMMARY OF THE INVENTION

[0009] The present invention is drawn to a method for modulating IL-13 expression and/or activity in a mammal, preferably a human, comprising administering an effective amount of an agent which modulates the expression and/or activity of IL-9. In a preferred embodiment IL-13 expression and/or activity is down-regulated.

[0010] In some embodiments of the invention the agent is an IL-9 antagonist. In a preferred embodiment the IL-9 antagonist is an antibody against IL-9 or the IL-9 receptor. In a further embodiment thereof, the antibody is a monoclonal antibody. In a preferred embodiment the antibody is a chimeric antibody and in a specific embodiment thereof, the chimeric antibody is a humanized antibody. In another embodiment the IL-9 antagonist is a soluble IL-9 receptor protein.

[0011] In a preferred embodiment the down-regulation of IL-13 alleviates at least one symptom associated with an atopic allergy and in a particularly preferred embodiment the atopic allergy is asthma. Examples of symptoms which can be alleviated by the method of the present invention include, but are not limited to, bronchial hyperresponsiveness, bronchoconstriction, bronchial inflammation, pulmonary fibrosis, eosinophilia, elevated serum IgE levels and mucin overproduction. In another embodiment, the down-regulation of IL-13 produces a down-regulation in 15-lipoxygenase expression and/or activity, or an up-regulation in isozyme 5-lipoxygenase expression and/or activity.

[0012] The present invention is also drawn to treating a disease associated with elevated levels of IL-13 in a mammal, preferably a human, comprising administration of an effective amount of an IL-9 antagonist. In a preferred embodiment the disease is an atopic allergy and in a particularly preferred embodiment the atopic allergy is asthma. In another preferred embodiment the disease is an infectious disease. In a specific embodiment, the disease is further associated with a Th1-type inflammatory response. In a preferred embodiment the IL-9 antagonist is an antibody against IL-9 or the IL-9 receptor. In a further embodiment thereof, the antibody is a monoclonal antibody. In a preferred embodiment the antibody is a chimeric antibody and in a specific embodiment thereof, the chimeric antibody is a humanized antibody. In another embodiment the IL-9 antagonist is a soluble IL-9 receptor protein.

[0013] In some embodiments of the present invention, the agent is administered by a route selected from the group consisting of intravenous, subcutaneous, transdennal, mucosal, intranasal, oral, bronchial adminstration. In a particular embodiment, the bronchial administration is carried out with an aerosol inhaler.

[0014] Another aspect of the present invention is a method of identifying an agent which modulates IL-13 expression and/or activity comprising contacting a cell expressing an IL-9 receptor with the agent in the presence of an IL-9 receptor ligand, and measuring the expression and/or activity of IL-13, wherein a decrease in IL-13 expression and/or activity indicates an agent capable of modulating IL-13 expression and/or activity. In some embodiments, the IL-9 receptor ligand is selected from the group consisting of IL-9 or a fragment thereof, an IL-9 analog and an IL-9 peptide mimetic.

BRIEF DESCRIPTION OF THE FIGURES

[0015]FIG. 1 depicts induction of IL-13 gene expression in transgenic mice overexpressing IL-9.

[0016]FIG. 2 depicts induction of IL-13 gene expression in IL-9 responsive cell lines and tissues of IL-9 transgenic mice.

[0017]FIG. 3 depicts inhibition of IL-13 up-regulation with neutralizing IL-9 antibody in a murine model of asthma.

[0018]FIG. 4 depicts inhibition of IL-13 up-regulation with a neutralizing IL-9 antibody versus a non-neutralizing IL-9 control antibody, and non-antibody-treated infective control animals in a murine model of asthma.

DETAILED DESCRIPTION OF THE INVENTION

[0019] General Description

[0020] The invention is based on the identification of IL-13 in the IL-9 pathway and methods for regulating the pathway which may be used in the treatment of diseases associated with IL-13. The invention includes methods of modulating IL-13 expression and/or activity by treating a subject with an agent which modulates the expression and/or activity of IL-9. Agents of the invention may be an anti-IL-9 antibody or anti-IL-9 receptor antibody, particularly a neutralizing antibody, soluble IL-9 receptor or fragments thereof, fragments of IL-9 which competitively inhibit IL-9 binding to the receptor, analogs of IL-9, and peptide mimetics of IL-9. The modulation of IL-13 is useful for the treatment of atopic allergies, including asthma. Methods for modulation of IL-13 are further useful for the treatment of infectious diseases.

[0021] Modulation of IL-13 Expression and/or Activity

[0022] IL-13 has been identified as a cytolcine protein that is associated with IL-9 and subsequent activity of a Th1-type immune response leading to inflammation. Specifically, the expression and activation of IL-13 is dependent upon the expression and activity of IL-9. The present invention therefore includes methods for modulating IL-13 expression and/or activity by modulating IL-9 expression and/or activity, including methods for modulating IL-9 signal transduction pathways via downstream membrane and cytoplasmic signaling proteins, to effect activation of a Th1-type immune response. Such methods will be useful in the treatment of disorders associated with diseases associated with a Th1-type immune responses. Because IL-9 receptor expression and activity also indirectly effects IL-13 expression and activity via a general feedback mechanism, the invention also includes methods for modulating IL-13 expression and activity by modulating IL-9 receptor expression and/or activity.

[0023] Modulation of the IL-9 and/or IL-9 receptor gene, gene fragments, or the encoded protein or protein fragments is useful in gene therapy to treat disorders associated with IL-13 defects. For increased expression of IL-13, expression of IL-9 and/or its receptor is increased. Expression vectors may be used to introduce IL-9 or the IL-9 receptor gene into a cell. In a preferred embodiment, IL-9 expression is decreased to decrease IL-13 expression and activity in diseases associated with Th1-type immune responses and inflammation. Expression vectors may be used to introduce inactive, variant forms of IL-9 or the IL-9 receptor gene into a cell as has been demonstrated with mutated, inactive forms of IL-9 and the IL-9 receptor with any of the mutations described in U.S. Pat. No. 6,037,149 or U.S. patent application Ser. No. 09/596,377 (these references herein incorporated by reference in their entirety). Such vectors generally have convenient restriction sites located near the promoter sequence to provide for the insertion of nucleic acid sequences. Transcription cassettes may be prepared comprising a transcription initiation region, the target gene or fragment thereof, and a transcriptional termination region The transcription cassettes may be introduced into a variety of vectors, e.g., plasmid, retrovirus, lentivirus, adenovirus and the like, where the vectors are able to transiently or stably be maintained in the cells, usually for a period of at least about one day, more usually for a period of at least about several days to several weeks.

[0024] Both active and inactive, variant forms of IL-9 gene or the IL-9 receptor gene or proteins may be introduced into tissues or host cells by any number of routes, including viral infection, microinjection, or fusion of vesicles. Jet injection may also be used for intramuscular administration, as described by Furth et al. (1992) Anal. Biochem. 205, 365-368. The DNA may be coated onto gold microparticles, and delivered intradermally by a particle bombardment device, or using a “gene gun” as described in the literature (see, for example, Tang et al. (1992) Nature 356, 152-154), where gold microprojectiles are coated with mutant IL-9 receptor DNA, then bombarded into skin cells.

[0025] In a further embodiment, the invention includes the down-regulation of IL-13 expression and/or activity by administering soluble IL-9 receptor protein that binds IL-9 (Renauld et al. (1992) Proc. Natl. Acad. Sci. USA 89, 5690-5694). These soluble proteins can be used to prevent the binding of IL-9 to cell bound receptor and act as an antagonist of IL-9. Soluble receptors have been used to bind cytokines or other ligands to regulate their function (Thomson (1998) Cytokine Handbook, Academic Press). A soluble receptor is a form of a membrane bound receptor that occurs in solution, or outside of the membrane. Soluble receptors may occur because the segment of the molecule which commonly associates with the membrane is absent. This segment is commonly referred to in the art as the transmembrane domain of the gene, or membrane binding segment of the protein. Thus, in one embodiment of the invention, a soluble receptor may represent a fragment or an analog of a membrane bound receptor. In another embodiment of the invention, the structure of the segment that associates with the membrane may be modified (e.g., DNA sequence polymorphism or mutation in the gene) so the receptor is not inserted into the membrane, or the receptor is inserted, but is not retained within the membrane. Thus, a soluble receptor, in contrast to the corresponding membrane bound form, differs in one or more segments of the gene or receptor protein that are important to its association with the membrane (Renauld et al. (1992) Proc. Natl. Acad. Sci. USA 89, 5690-5694; Chang et al. (1994) Blood 83, 3199-3205).

[0026] These soluble receptors may be known forms of a soluble IL-9 receptor that act to bind IL-9. Alternatively, these soluble receptors may contain variations but still resemble known forms of the IL-9 receptor, and may exist as fragments. Examples of variant soluble IL-9 receptors and fragments thereof can be found in U.S. Pat. No. 6,037,149 and U.S. patent application Ser. No. 09/596,377 (these references herein incorporated by reference in their entirety). In another embodiment of the invention, the compound may retain functions comparable to soluble IL-9 receptor, but may not resemble soluble IL-9 receptor in composition. For example, the composition of the compound may include molecules other than amino acids. Thus, these compounds will bind IL-9 and prevent IL-9 from acting at its cell surface receptor.

[0027] Antisense molecules can be used to down-regulate expression of IL-9 or IL-9 receptor expression in cells. The anti-sense reagent may be antisense oligonucleotides, particularly synthetic antisense oligonucleotides having chemical modifications from native nucleic acids, or nucleic acid constructs that express such anti-sense molecules as RNA. The antisense sequence is complementary to the mRNA of the targeted gene, and inhibits expression of the targeted gene products. Antisense molecules inhibit gene expression through various mechanisms, e.g., by reducing the amount of mRNA available for translation, through activation of RNAseH or steric hindrance. One or a combination of antisense molecules may be administered, where a combination may comprise multiple different sequences.

[0028] Antisense molecules may be produced by expression of all or a part of the target gene sequence in an appropriate vector, where the transcriptional initiation is oriented such that an antisense strand is produced as an RNA molecule. Alternatively, the antisense molecule is a synthetic oligonucleotide. Antisense oligonucleotides will range from five to seventy-five and generally be at least about seven, usually at least about twelve, and more usually at least about twenty nucleotides in length. Typical antisense oligonucleotides are usually not more than about five-hundred, more usually not more than about fifty, and even more usually not more than about thirty-five nucleotides in length, where the length is governed by efficiency of inhibition, specificity, including absence of cross-reactivity, and the like. It has been found that short oligonucleotides, from seven to eight bases in length, can be strong and selective inhibitors of gene expression (see Wagner et al. (1996) Nat. Biotech. 14, 840-844).

[0029] A specific region or regions of the endogenous sense strand mRNA sequence is chosen to be complemented by the antisense sequence. Selection of a specific sequence for the oligonucleotide may use an empirical method, where several candidate sequences are assayed for inhibition of expression of the target gene in an in vitro or animal model. A combination of sequences may also be used, where several regions of the mRNA sequence are selected for antisense complementation.

[0030] Antisense oligonucleotides may be chemically synthesized by methods known in the art (see Wagner et al. (1996) Nat. Biotech. 14, 840-844). Preferred oligonucleotides are chemically modified from the native phosphodiester structure, in order to increase their intracellular stability (e.g., resistance to nuclease degradation and acid resistance) and binding affinity. A number of such modifications have been described in the literature, which alter the chemistry of the backbone, sugars or heterocyclic bases.

[0031] As an alternative to anti-sense inhibitors, catalytic nucleic acid compounds, e.g., ribozymes, deoxyribozymes (see, for example, Santoro et al. (1997) Proc. Natl. Acad. Sci. USA 94, 4262-4266), anti-sense conjugates, etc. may be used to inhibit gene expression. Ribozymes may be synthesized in vitro and administered to the patient, or may be encoded on an expression vector, from which the ribozyme is synthesized in the targeted cell (see, for example, WO 95/23225; Beigelman et al. (1995) Nuc. Acids Res. 23, 4434-4442). Examples of oligonucleotides with catalytic activity are described in WO 95/06764.

[0032] Methods of Treatment Associated with Modulation of IL-13 Expression

[0033] As provided in the Examples, the IL-13 protein and nucleic acid are expressed in response to stimulation by IL-9. Agents that modulate or up- or down-regulate the expression of the IL-9 protein or agents such as agonists or antagonists of at least one activity of the IL-9 or IL-9 receptor protein may be used to modulate biological, and pathologic processes associated with IL-13 function and activity in a subject. As used herein, a “subject” can be any mammal, so long as the mammal is in need of modulation of a pathological or biological process mediated by a protein of the invention. The term “mammal” is defined as an individual belonging to the class Mammalia. The invention is particularly useful in the treatment of human subjects.

[0034] Pathological processes refer to a category of biological processes which produce a deleterious effect. For example, increased IL-13 expression and/or activity is associated with diseases characterized by a Th1-type immune response leading to inflammation. Such diseases include, but are not limited to, atopic allergy. As used herein, the term “atopic allergy” refers to atopy and related disorders including asthma, bronchial hyperresponsiveness, rhinitis, urticaria, allergic inflammatory disorders of the bowel and various forms of eczema. Atopy is a hypersensitivity to environmental allergens expressed as the elevation of serum total IgE or abnormal skin test responses to allergens as compared to controls. Atopic allergies include conditions where there is a genetic predisposition toward the development of immediate (type I) hypersensitivity reactions against common environmental antigens. Bronchial hyperresponsiveness is characterized by a heightened bronchoconstrictor response to a variety of external stimuli.

[0035] Modulation of IL-13 expression can therefore be used to treat different types of atopic allergy and symptoms associated with types of atopic allergy. Symptoms of atopic allergy include, but are not limited to, bronchial hyperresponsiveness, bronchoconstriction, bronchial inflammation, pulmonary fibrosis, eosinophilia, elevated serum IgE levels and mucin overproduction. Examples of atopic allergy treatable by the present method include, but are not limited to, allergic rhinitis, bronchial asthma, atopic dermatitis, food allergies, allergies to animal dander or products, pollen allergies, and dust allergies.

[0036] As discussed above, those skilled in the art will appreciate that a wide variety of conditions are associated with IL-9 dependent increases in IL-13 expression and/or activity. Asthma is an example of one such atopic allergy characterized by increased IL-13 expression and/or activity associated with IL-9. As used herein, the term “asthma” encompasses inflammatory disorders of the airways with reversible airflow obstruction. The term further refers to conditions marked by recurrent attacks of paroxysmal dyspnea, with wheezing due to spasmodic contraction of the bronchii. Some cases of asthma are allergic manifestations in sensitized persons (bronchial allergy); others are provoked by a variety of factors including, but not limited to, exercise, irritant particles, animal dander, pollen, and psychological stress. Symptoms of asthma include, but are not limited to, bronchial hyperresponsiveness, bronchoconstriction, bronchial inflammation, pulmonary fibrosis, eosinophilia, elevated serum IgE levels and mucin overproduction.

[0037] As used herein, an agent is said to modulate a pathological process when the agent reduces the degree or severity of the process. For instance, a disorder associated with IL-13 expression may be prevented or disease progression modulated by the administration of agents which reduce, promote or modulate in some way the expression or at least one activity of IL-9 or its receptor. For atopic allergy, including asthma, the therapeutic strategy comprises a treatment with the agent until the aforementioned symptoms associated with atopic allergy, including asthma, are alleviated. Then the treatment can be switched to established regimens for the prevention of atopic allergy, including asthma, to avoid potential side effects of IL-13 levels which are below normal.

[0038] Other embodiments of the present invention allow for the treatment of other conditions that involve IL-13 expression. For example, many types of infectious disease are associated with elevated levels of IL-13. High levels of IL-13 have also associated with diseases that are characterized by fibrosis such as Hodgkin's disease. A decrease in IL-13 expression and/or activity through inhibition of IL-9 can be useful to decrease Th1-type immune responses associated with these diseases. Organisms responsible for, or contributing to, infectious diseases treatable by the present methods include, but are not limited to, viruses, bacteria, protozoa, fungi, and parasites. Examples of infectious disease include, but are not limited to, myobacterium tuberculosis, hemorrhagic fever, etc.

[0039] The invention also includes pharmaceutical compositions comprising the agents of the invention together with a pharmaceutically acceptable carrier. Pharmaceutically acceptable carriers can be sterile liquids, such as water and oils, including those of petroleum, animal, vegetable or synthetic origin, such as peanut oil, soybean oil, mineral oil, sesame oil and the like. Water is a preferred carrier when the pharmaceutical composition is administered intravenously. Saline solutions and aqueous dextrose and glycerol solutions can also be employed as liquid carriers, particularly for injectable solutions. Suitable pharmaceutical carriers are described in Remington's Pharmaceutical Sciences, Mack Publishing (1995).

[0040] The agents used in the method of treatment of this invention may be administered systemically, topically or enterally, depending on such considerations as the condition to be treated, need for site-specific treatment, quantity of drug to be administered and similar considerations. Indeed, all three types of formulations may be used simultaneously to achieve systemic administration of the active ingredient.

[0041] Topical administration may be used. Any common topical formation, such as a solution, suspension, gel, ointment or salve and the like may be employed. Preparation of such topical formulations are well described in the art of pharmaceutical formulations as exemplified, for example, by Gennaro et al. (1995) Remington's Pharmaceutical Sciences, Mack Publishing. For topical application, these agents could also be administered as a powder or spray, particularly in aerosol form. The active ingredient may be administered in pharmaceutical compositions adapted for systemic administration. As is known, if a drug is to be administered systemically, it may be confected as a powder, pill, tablet or the like or as a syrup or elixir for oral administration. Preparations for oral administration may be suitably formulated to give controlled release of the active compound.

[0042] The agents used in the method of treatment of this invention may be formulated for parenteral administration by injection, e.g., by bolus injection or continuous infusion. As used herein, the term “parenteral” refers to routes of administration including, but not limited to, intravenous, intraperitoneal, intra-lesional, subcutaneous, intradermal, intramuscular, intracapsular, and direct injection into mucosal tissues. Formulations for injection may be presented in unit dosage form, e.g., in ampoules or in multi-dose containers. The agents may take such forms as suspensions, solutions or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilizing and/or dispersing agents. Alternatively, the active ingredient may be in powder form for constitution with a suitable vehicle, e.g., sterile pyrogen-free water, before use.

[0043] In some embodiments, the agents may also be formulated in rectal compositions such as suppositories or retention enemas, e.g., containing conventional suppository bases such as cocoa butter or other glycerides. In some embodiments, the agents may also be formulated as a depot preparation. Such long acting formulations may be administered by implantation (for example, subcutaneously or intramuscularly) or by intramuscular injection. Thus, for example, the compounds may be formulated with suitable polymeric or hydrophobic materials (for example, as an emulsion in an acceptable oil) or ion exchange resins, or as sparingly soluble derivatives, for example, as a sparingly soluble salt. Liposomes and emulsions are well known examples of delivery vehicles or carriers for hydrophilic drugs.

[0044] In some embodiments of the present invention, the route of administration of agents for use in the present invention is in an aerosol or inhaled form administered using any appropriate inhaler, insufflator or inhalation device known in the art including, but not limited to, a nebulizer, a pressurized metered dose inhaler (MDI), or a dry powder inhaler, for example. The agents can be administered as dry powder particles or as an atomized aqueous solution suspended in a carrier gas. In a related embodiment, the invention includes administration by bronchial lavage, wherein the agent in instilled in an effective amount in the fluid to be administered to the lungs via ravage.

[0045] Dry aerosol in the form of finely divided solid particles of agents for use according to the present invention that are not dissolved or suspended in a liquid can be administered using a dry powder inhaler, such as those well known in the art. The agent may be in the form of dusting powders and comprise finely divided particles having an average particle size of between about 1 and 5 microns, preferably between 2 and 3 microns. Finely divided particles may be prepared by pulverization and screen filtration using techniques well known in the art. Capsules and cartridges of, e.g., gelatin for use in an inhaler or insufflator may be formulated containing a powder mix of the compound and a suitable powder base, e.g., lactose or a starch. The particles may be administered by inhaling a predetermined quantity of the finely divided material, which can be in the form of a powder.

[0046] Agents for use according to the present invention may be administered comprised in pharmaceutical formulations in the form of an aerosol spray using for example, a nebulizer, wherein the agent is dispersed as an atomized aqueous solution suspended in a carrier gas (e.g., air, N₂, CO₂, dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, or other suitable gas) and the aerosol material is inhaled by the subject to be treated. Preferred aerosol pharmaceutical formulations may comprise for example, a physiologically-acceptable buffered saline solution containing between about 1 mg and about 300 mg of the antigens. Specific non-limiting examples of the carriers and/or diluents that are useful in the by-inhalation pharmaceutical formulations include water and physiologically-acceptable buffered solutions such as cromolyn sodium or phosphate buffered saline solutions pH 7.0-8.0.

[0047] As used herein, an “effective amount” of an agent of the invention is that amount which will change the level of IL-13. Preferably, an effective amount is that amount which will significantly change the level of IL-13. Also preferably, an effective amount is that amount which will change the level of IL-13 by at least about ten percent, more preferably by at least about twenty percent, even more preferably by at least about thirty percent, yet more preferably by at least about forty percent, still more preferably by at least about fifty percent, even still more preferably by at least about sixty percent, yet still more preferably by at least about seventy percent, still further more preferably by at least about eighty percent, yet further more preferably by at least about ninety percent, and in a particularly preferable embodiment by at least about ninety-five percent. Most preferably, an effective amount is that amount which will change the level of IL-13 by at least about ninety-nine percent. A given effective amount will vary from condition to condition and in certain instances may vary with the severity of the condition being treated and the patient's susceptibility to treatment. Accordingly, a given effective amount will be best determined at the time and place through routine experimentation. However, it is anticipated that in the treatment of atopic allergy and asthma-related disorders and other diseases, in accordance with the present invention, a formulation containing between 0.001 and 5.0 percent by weight, preferably about 0.01 to 1.0 percent, will usually constitute a therapeutically effective amount. When administered systemically, an amount between 0.01 and 100 milligrams per kilogram body weight per day, but preferably about 0.1 to 10 milligrams per kilogram, will effect a therapeutic result in most instances.

[0048] In practicing the methods of this invention, the agents of the invention may be used alone or in combination, or in combination with other therapeutic or diagnostic agents. In certain preferred embodiments, the agents of the invention may be co-administered along with other compounds typically prescribed for conditions according to generally accepted medical practice. For example, an agent of the present invention can be administered in combination with other drugs for the treatment of atopic allergy, including asthma, related disorders, or other drugs for the treatment of infective diseases. As used herein, two agents are said to be administered in combination when the two agents are administered simultaneously or are administered independently in a fashion such that the agents will act at the same time. The agents of this invention can be utilized in vivo in mammals, such as humans, sheep, horses, cattle, pigs, dogs, cats, rats and mice, or in vitro.

[0049] The present invention also includes antagonists of IL-9 and its receptor, such as disclosed in U.S. Pat. No. 6,261,559 (herein incorporated by reference in its entirety). In particularly preferred embodiments, an antagonist of IL-9 or its receptor is an agent that, though its effect on the IL-9 pathway, inhibits the up-regulation of IL-13 expression in response to a stimulus. Antagonists are compounds that cause effects by preventing the action of an agonist. IL-9 antagonists of the present invention include, but are not limited, neutralizing antibodies to IL-9, antibodies to IL-9 receptor, agents which competitively bind to the IL-9 receptor without activation of the receptor, soluble forms of the IL-9 receptor, and fragments of the IL-9 receptor which prevent IL-9 binding to IL-9 receptor. These and further antagonists of the invention may be tested for competitive binding with a known agonist, or for down-regulation of IL-9-like functions as described in U.S. Pat. No. 6,261,559 and the references cited therein. The binding of either the agonist or antagonist may involve all known types of interactions including ionic forces, hydrogen bonding, hydrophobic interactions, van der Waals forces, and covalent bonds. In many cases, bonds of multiple types are important in the interation of an agonist or antagonist with a receptor.

[0050] In a further embodiment, agents of the invention may be analogs of IL-9. Such analogs may be produced by point mutations in the isolated DNA sequence for the gene, nucleotide substitutions, and/or deletions which can be created by methods that are all well described in the art (see, e.g., Simoncsits et al. (1994) Cytoline 6, 206-214). This invention also includes splice variants of IL-9 which contain deletions of one or more of its five exons as disclosed in related U.S. Pat. No. 6,261,559. The term “splice variants” as used herein denotes a purified and isolated DNA molecule encoding human IL-9 comprising at least one exon. There is no evidence of naturally expressed spliced mutants in the art. Thus, the agents of the present invention can include a protein encoded by an isolated nucleic acid containing exons 1, 4 and 5 of human IL-9. Other variants within the scope of this invention include sequences comprising exons 1, 2, 3, 4 and 5; exons 1, 2, 3 and 4; exons 1, 2, 4 and 5 and exons 1, 3, 4 and 5. It is understood that these exons may contain various point mutations.

[0051] Specific examples of antagonistic peptides derived from IL-9 include KP-16 (SEQ ID NO: 15) and KP-20 (SEQ ID NO: 16) which are derived from exon 4. Exon 4 encodes forty-four amino acids while the peptides mentioned above contain sixteen and twenty amino acids respectively and they do not overlap. These peptides exhibit considerable inhibitory activity both individually and when assayed in combination. Additionally, KP-23 (SEQ ID NO: 17) and KP-24 (SEQ ID NO: 18) are derived from exon 5 and also exhibit similar activity. The sequences of KP-16, KP-20, KP-23 and KP-24 are disclosed in U.S. Pat. No. 6,037,149 (herein incorporated by reference in its entirety). Splice variants of IL-9 can be formed by deletion of any one or more of the IL-9 exons 1 through 5. As shown above, peptides derived from these exons show regulatory capability and, accordingly, are useful in treating atopic allergies, including asthma.

[0052] In another embodiment, the agents of the invention are antibodies to IL-9 or the IL-9 receptor. As used herein, the term “antibody” refers to immunoglobulins and is used in the broadest sense, including monoclonal antibodies, polyclonal antibodies, multispecific antibodies (e.g., bispecific antibodies) and antibody fragments. An antibody is said to “recognize” an epitope if it binds to the epitope. Hence, “recognition” involves the antibody binding reaction with an epitope, which may include the typical binding mechanisms and methods. “Binding” is thus used in the conventional sense, and does not require the formation of chemical bonds.

[0053] As used herein, the term “antibody fragments” refers to a portion of a full length antibody capable of binding an epitope, generally the antigen binding or variable region thereof. Examples of antibody fragments include Fab, Fab′ and F(ab′)₂ or Fv fragments; diabodies; linear antibodies; single-chain antibody molecules; and multispecific antibodies formed from antibody fragments.

[0054] As used herein, the term “monoclonal antibody” refers to an antibody obtained from a population of substantially homogeneous antibodies (i.e., the individual antibodies comprising the population are identical except for possible naturally occurring mutations that may be present in minor amounts). Monoclonal antibodies are highly specific, being directed against a single antigenic site. Furthermore, in contrast to conventional (polyclonal) antibody preparations which typically include different antibodies directed against different determinants (epitopes), each monoclonal antibody is directed against a single determinant on the antigen. The modifier “monoclonal” indicates the character of the antibody as being obtained from a substantially homogeneous population of antibodies, and is not to be construed as requiring production of the antibody by any particular method. For example, the monoclonal antibodies to be used in accordance with the present invention may be made by the hybridoma method first described by Kohler et al. (1975) Nature 256, 495497 or may be made by recombinant DNA methods (see, e.g., U.S. Pat. No. 4,816,567). The monoclonal antibodies may also be isolated from phage antibody libraries using the techniques described in, for example, Clackson et al. (1991) Nature 352, 624-628 and Marks et al. (1991) J. Mol. Biol. 222, 581-597.

[0055] Monoclonal antibodies specifically include “chimeric” antibodies (immunoglobulins) in which a portion of the heavy and/or light chain is identical with, or homologous to corresponding sequences in antibodies derived from a particular species, or belonging to a particular antibody class or subclass, while the remainder of the chain(s) is identical with, or homologous to corresponding sequences in antibodies derived from another species or belonging to another antibody class or subclass, as well as fragments of such antibodies (see, e.g., U.S. Pat. No. 4,816,567 and Morrison et al. (1984) Proc. Natl. Acad. Sci. USA 81, 6851-6855). Chimeric antibodies also include “humanized” antibodies, as well as fragments of such antibodies, wherein the antigen-recognized sites, or complementarily-determining hypervariable regions (CDR) are of non-human origin, whereas framework regions (FR) of variable domains and constant regions are products of human genes. Said CDR and FR regions may comprise amino-acid alterations in order to adjust the binding affinity of the humanized antibody (see, e.g., Gussow et al. (1991) Meth. Enzymol. 203, 99-121).

[0056] The antibodies to IL-9 and the IL-9 receptor may be either monoclonal or polyclonal made using standard techniques well known in the art (Harlow & Lane (1988) Antibodies, A Laboratory Manual, Cold Spring Harbor Laboratory Press). They can be used to block IL-9 from binding to the receptor. In one embodiment the antibodies interact with IL-9. In another embodiment the antibodies interact with the IL-9 receptor. The IL-9 used to elicit these antibodies can be any of the IL-9 variants discussed above. Antibodies are also produced from peptide sequences of IL-9 or the IL-9 receptor using standard techniques in the art (Harlow & Lane (1988) Antibodies, A Laboratory Manual, Cold Spring Harbor Laboratory Press). Examples of peptide sequences from the IL-9 receptor that can be used to produce blocking antisera are disclosed in U.S. Pat. No. 6,037,149. IL-9 and IL-9 receptor sequences comprising epitopes from murine sequences are also useful for the production of therapeutic antibodies.

[0057] In another aspect of the invention, aminosterol compounds are also useful in the inhibition of signal transduction due to IL-9 stimulation. Specifically, aminosterol compounds can be used to down-regulate IL-9 expression and/or activity leading to a decrease in IL-13 expression and/or activity. Aminosterol compounds which are useful in this invention are described in U.S. Pat. No. 5,637,691 and its related U.S. Pat. Nos. 5,733,899 and 5,721,226 as well as in U.S. Pat. No. 5,840,740 and its related U.S. Pat. Nos. 5,795,885; 5,994,336; 5,763,430; 5,840,936; 5,874,597; 5,792,635 and 5,847,172 (which are specifically incorporated herein by reference in their entirety).

[0058] Screening for Agents which Modulate IL-13 Expression

[0059] Another embodiment of the present invention provides methods for identifying agents that modulate the expression of a nucleic acid encoding a IL-13 protein whose expression is dependent upon IL-9. Such assays may utilize any available means of monitoring for changes in the expression level of the nucleic acids encoding IL-13, IL-9 and/or IL-9 receptor proteins. As used herein, an agent is said to modulate the expression of a nucleic acid encoding a IL-13 protein, if it is capable of up- or down-regulating expression of the nucleic acid in a cell.

[0060] In one assay format, cell lines that contain reporter gene fusions between any region of the open reading frame of the IL-13 gene or fragments thereof under control of the gene's promoter and any assayable fusion partner. Numerous assayable fusion partners are known and readily available including the firefly luciferase gene and the gene encoding chloramphenicol acetyltransferase (Alam et al. (1990) Anal. Biochem. 188, 245-254). Cell lines containing the reporter gene fusions are then exposed to the agent to be tested under appropriate conditions and time. Differential expression of the reporter gene between samples exposed to the agent and control samples identifies agents which modulate the expression of a nucleic acid encoding a IL-13 protein.

[0061] Additional assay formats may be used to monitor the ability of the agent to modulate the expression of a nucleic acid encoding a IL-13 protein associated with IL-9 expression and activity. For instance, mRNA expression may be monitored directly by hybridization to the nucleic acids encoding the IL-13, IL-9 and IL-9 receptor gene. Cell lines are exposed to the agent to be tested under appropriate conditions and time and total RNA or mRNA is isolated by standard procedures such those disclosed in Sambrook et al. (1989) Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press.

[0062] Probes to detect differences in RNA expression levels between cells exposed to the agent and control cells may be prepared from the nucleic acids encoding the IL-13, IL-9 or IL-9 receptor gene. It is preferable, but not necessary, to design probes which hybridize only with target nucleic acids under conditions of high stringency. Only highly complementary nucleic acid hybrids form under conditions of high stringency. Accordingly, the stringency of the assay conditions determines the amount of complementarily which should exist between two nucleic acid strands in order to form a hybrid. Stringency should be chosen to maximize the difference in stability between the probe:target hybrid and potential probe:non-target hybrids.

[0063] Probes may be designed from the nucleic acids encoding the IL-13, IL-9 and/or IL-9 receptor gene through methods known in the art. For instance, the G+C content of the probe and the probe length can affect probe binding to its target sequence. Methods to optimize probe specificity are commonly available in Sambrook et al. (1989) Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press; or Ausubel et al. (1995) Current Protocols in Molecular Biology, Greene Publishing Company.

[0064] Hybridization conditions are modified using known methods, such as those described by Sambrook et al. (1989) Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press; or Ausubel et al. (1995) Current Protocols in Molecular Biology, Greene Publishing Company as required for each probe. Hybridization of total cellular RNA or RNA enriched for polyadenylated RNA can be accomplished in any available format. For instance, total cellular RNA or RNA enriched for polyadenylated RNA can be affixed to a solid support and the solid support exposed to at least one probe comprising at least one, or part of one of the sequences encoding the IL-13, IL-9 and/or IL-9 receptor gene under conditions in which the probe will specifically hybridize.

[0065] Alternatively, nucleic acid fragments comprising at least one, or part of one of the sequences of the invention can be affixed to a solid support, such as a porous glass wafer. The glass wafer can then be exposed to total cellular RNA or polyadenylated RNA from a sample under conditions in which the affixed sequences will specifically hybridize. Such glass wafers and hybridization methods are widely available, for example, those disclosed in WO 95/11755. By examining for the ability of a given probe to specifically hybridize to an RNA sample from an untreated cell population and from a cell population exposed to the agent, agents which up or down regulate the expression of a nucleic acid (SEQ ID NO: 11 for human or SEQ ID NO: 13 for murine) encoding the IL-13 protein (SEQ ID NO: 12 for human or SEQ ID NO: 14 for murine) are identified.

[0066] Hybridization for qualitative and quantitative analysis of mRNA may also be carried out by using a RNase Protection Assay (i.e., RPA, see Ma et al. (1996) Methods 10, 273-238). Briefly, an expression vehicle comprising cDNA encoding the gene product and a phage specific DNA dependent RNA polymerase promoter (e.g., T7, T3 or SP6 RNA polymerase) is linearized at the 3′ end of the cDNA molecule, downstream from the phage promoter, wherein such a linearized molecule is subsequently used as a template for synthesis of a labeled antisense transcript of the cDNA by in vitro transcription. The labeled transcript is then hybridized to a mixture of isolated RNA (i.e., total or fractionated mRNA) by incubation at 45° C. overnight in a buffer comprising eighty percent formamide, 40 mM Pipes (pH 6.4), 0.4 M NaCl and 1 mM EDTA. The resulting hybrids are then digested in a buffer comprising 40 mg/ml ribonuclease A and 2 mg/ml ribonuclease. After deactivation and extraction of extraneous proteins, the samples are loaded onto urea/polyacrylamide gels for analysis.

[0067] In another assay format, agents which effect the expression of the instant gene products, cells or cell lines would first be identified which express said gene products physiologically. Cells and cell lines so identified, such as cells derived from the lung, would be expected to comprise the necessary cellular machinery such that the fidelity of modulation of the transcriptional apparatus is maintained with regard to exogenous contact of agent with appropriate surface transduction mechanisms and/or the cytosolic cascades. Further, such cells or cell lines would be transduced or transfected with an expression vehicle (e.g., a plasmid or viral vector) construct comprising an operable non-translated 5′-promoter upstream of the structural gene encoding the instant gene products fused to one or more antigenic fragments, which are peculiar to the instant gene products, wherein said fragments are under the transcriptional control of said promoter and are expressed as polypeptides whose molecular weight can be distinguished from the naturally occurring polypeptides or may further comprise an immunologically distinct tag. Such a process is well known in the art (see Sambrook et al. (1989) Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press).

[0068] Cells or cell lines transduced or transfected as outlined above would then be contacted with agents under appropriate conditions; for example, the agent comprises a pharmaceutically acceptable excipient and is contacted with cells comprised in an aqueous physiological buffer such as phosphate buffered saline (PBS) at physiological pH, Eagles balanced salt solution (BSS) at physiological pH, PBS or BSS comprising serum or conditioned media comprising PBS or BSS and/or serum incubated at 37° C. Said conditions may be modulated as deemed necessary by one of skill in the art. Subsequent to contacting the cells with the agent, said cells will be disrupted and the polypeptides from disrupted cells are fractionated such that a polypeptide fraction is pooled and contacted with an antibody to be further processed by immunological assay (e.g., ELISA, immunoprecipitation or Western blot). The pool of proteins isolated from the “agent contacted” sample will be compared with a control sample where only the excipient is contacted with the cells and an increase or decrease in the immunologically generated signal from the “agent contacted” sample compared to the control will be used to distinguish the effectiveness of the agent.

[0069] Methods to Identify Agents that Modulate IL-13 Activity

[0070] The present invention provides methods for identifying agents that modulate at least one activity of a IL-13 protein associated with IL-9 expression and activity. Such methods or assays may utilize any means of monitoring or detecting the desired activity.

[0071] In one format, the specific activity of a IL-13 protein, normalized to a standard unit, between a cell population that has been exposed to the agent to be tested compared to an un-exposed control cell population may be assayed. Cell lines or populations are exposed to the agent to be tested under appropriate conditions and time. Cellular lysates may be prepared from the exposed cell line or population and a control, unexposed cell line or population. The cellular lysates are then analyzed with the probe.

[0072] Other screening assays may include measuring IL-13 activity by determining IL-9 and/or IL-9 receptor expression and/or activity. This could be accomplished by screening agents in cells containing IL-13 and IL-9 and/or the IL-9 receptor, determining IL-9 expression and/or activity by an appropriate method, and then screening agents in cell line not expressing IL-13 as a negative control. Agents which could act through IL-9 activation of IL-13 would be those increasing IL-9 and IL-13 expression in a IL-13-positive cell line, but not in a IL-13-negative cell line. 15-lipoxygenase and its isozyme 5-lipoxygenase activity assays could also be used where cells are stimulated with screening agents followed by exposure of the cell lysate (or sub-lysate fraction) to a specific lipoxygenase substrate to monitor the activation of intrinsic lipoxygenase activity. The association of specific binding proteins with IL-13 (e.g., IL-13 receptor) could also be used as an indication of IL-9 dependent activation of IL-13.

[0073] In yet another embodiment, one could test agents to identify which agents bind to IL-9 or its receptor to increase IL-13 expression and/or activity. Methods of determining binding of an agent to a receptor are well known in the art. Typically, the assays include the steps of incubating a source of the IL-9 or its receptor with a labeled agent, known to bind to IL-9 or its receptor, in the presence or absence of a test agent and determining the amount of bound labeled agent. The source of IL-9 receptor may either be cells expressing IL-9 receptor or some form of isolated IL-9 receptor as described herein. Cells expressing IL-9 receptor can be either cells which naturally express the IL-9 receptor or cells which have been engineered to express IL-9 receptor. Methods of recombinantly engineering a cell to express a protein such as IL-9 receptor are well Inown to those in the art. The labeled agent can be IL-9 or any IL-9 analog labeled such that it can be measured quantitatively (e.g., fluorescein labeled, GFP labeled, radiolabeled or europium labeled). Test agents that bind to the IL-9 receptor cause a reduction in the amount of labeled agent bound to the receptor, thereby reducing the signal level compared to that from control samples (absence of test compound). Binding of an agent to the IL-9 receptor can be used as an indicator of agents capable of inhibiting IL-9-dependent IL-13 expression and/or activity.

[0074] Antibody probes can be prepared by immunizing suitable mammalian hosts utilizing appropriate immunization protocols using the IL-9 and/or IL-9 receptor protein or antigen-containing fragments thereof. To enhance immunogenicity, these proteins or fragments can be conjugated to suitable carriers. Methods for preparing immunogenic conjugates with carriers such as BSA, KLH or other carrier proteins are well known in the art. In some circumstances, direct conjugation using, for example, carbodiimide reagents may be effective; in other instances linking reagents such as those supplied by Pierce Chemical Co. may be desirable to provide accessibility to the hapten. The hapten peptides can be extended at either the amino or carboxy terminus with a cysteine residue or interspersed with cysteine residues, for example, to facilitate linking to a carrier. Administration of the immunogens is conducted generally by injection over a suitable time period and with use of suitable adjuvants, as is generally understood in the art. During the immunization schedule, titers of antibodies are taken to determine adequacy of antibody formation.

[0075] While the polyclonal antisera produced in this way may b& satisfactory for some applications, use of monoclonal preparations is preferred for antibody probes. Immortalized cell lines which secrete the desired monoclonal antibodies may be prepared using standard methods, see e.g., Kohler & Milstein (1992) Biotechnology 24, 524-526 or modifications which effect immortalization of lymphocytes or spleen cells, as is generally known. The immortalized cell lines secreting the desired antibodies can be screened by immunoassay in which the antigen is the peptide hapten, polypeptide or protein. When the appropriate immortalized cell culture secreting the desired antibody is identified, the cells can be cultured either in vitro or by production in ascites fluid.

[0076] The desired monoclonal antibodies may be recovered from the culture supernatant or from the ascites supernatant. The intact antibodies or fragments thereof which contain the immunologically significant portion can be used as e.g., antagonists of binding between IL-9 (ligand) and its receptor, or alternatively as a IL-9 receptor agonists. Use of immunologically reactive fragments, such as Fab or Fab′ fragments, is often preferable, especially for antibody probes, as these fragments are generally less immunogenic than the whole immunoglobulin. The antibodies or fragments may also be produced, using current technology, by recombinant means. Antibody regions that bind specifically to the desired regions of the protein can also be produced in the context of chimeras with multiple species origin.

[0077] Antibody regions that bind specifically to the desired regions of the IL-9 receptor can also be produced in the context of chimeras with multiple species origin, for instance, humanized antibodies. The antibody probes can therefore be a humanized antibody or a human antibody, as described in U.S. Pat. No. 5,585,089 or Riechmann et al. (1988) Nature 332, 323-327.

[0078] Agents that are assayed in the above method can be randomly selected or rationally selected or designed. As used herein, an agent is said to be randomly selected when the agent is chosen randomly without considering the specific sequences involved in the association of the a protein of the invention alone or with its associated substrates, binding partners, etc. An example of randomly selected agents is the use a chemical library or a peptide combinatorial library, or a growth broth of an organism.

[0079] As used herein, an agent is said to be rationally selected or designed when the agent is chosen on a non-random basis which takes into account the sequence of the target site or its conformation in connection with the agent's action. Agents can be rationally selected or rationally designed by utilizing the peptide sequences that make up these sites. The agents of the present invention can be, as examples, peptides, peptide mimetics, antibodies, antibody fragments, small molecules, vitamin derivatives, as well as carbohydrates. Peptide agents of the invention can be prepared-using standard solid phase (or solution phase) peptide synthesis methods, as is known in the art. In addition, the DNA encoding these peptides may be synthesized using commercially available oligonucleotide synthesis instrumentation and produced recombinantly using standard recombinant production systems. The production using solid phase peptide synthesis is necessitated if non-gene-encoded amino acids are to be included.

[0080] Another class of agents of the present invention are antibodies or fragments thereof that bind to IL-9 or the IL-9 receptor protein. Antibody agents can be obtained by immunization of suitable mammalian subjects with peptides, containing as antigenic regions, those portions of the protein intended to be targeted by the antibodies.

[0081] In yet another class of agents, the present invention includes peptide mimetics which mimic the three-dimensional structure of IL-9 and bind to the IL-9 receptor. Such peptide mimetics may have significant advantages over naturally-occurring peptides, including, for example: more economical production, greater chemical stability, enhanced pharmacological properties (half-life, absorption, potency, efficacy, etc.), altered specificity (e.g., a broad-spectrum of biological activities), reduced antigenicity and others.

[0082] In one form, mimmetics are peptide-containing molecules that mimic elements of protein secondary structure. The underlying rationale behind the use of peptide mimetics is that the peptide backbone of proteins exists chiefly to orient amino acid side chains in such a way as to facilitate molecular interactions, such as those of antibody and antigen. A peptide mimetic is expected to permit molecular interactions similar to the natural molecule.

[0083] In another form, peptide analogs are commonly used in the pharmaceutical industry as non-peptide drugs with properties analogous to those of the template peptide. These types of non-peptide compounds are also referred to as peptide mimetics or peptidomimetics (Fauchere (1986) Adv. Drug Res. 15, 29-69; Veber & Freidinger (1985) Trends Neurosci. 8, 392-396; Evans et al. (1987) J. Med. Chem. 30, 1229-1239 which are incorporated herein by reference) and are usually developed with the aid of computerized molecular modeling.

[0084] Peptide mimetics that are structurally similar to therapeutically useful peptides may be used to produce an equivalent therapeutic or prophylactic effect Generally, peptide mimetics are structurally similar to a paradigm polypeptide (i.e., a polypeptide that has a biochemical property or pharmacological activity), such as the binding domain of IL-9, but have one or more peptide linkages optionally replaced by a linkage by methods known in the art.

[0085] Labeling of peptide mimetics usually involves covalent attachment of one or more labels, directly or through a spacer (e.g., an amide group), to non-interfering position(s) on the peptide mimetic that are predicted by quantitative structure-activity data and molecular modeling. Such non-interfering positions generally are positions that do not form direct contacts with the macromolecule(s) to which the peptide mimetic binds to produce the therapeutic effect. Derivitization (e.g., labeling) of peptide mimetics should not substantially interfere with the desired biological or pharmacological activity of the peptide mimetic.

[0086] The use of peptide mimetics can be enhanced through the use of combinatorial chemistry to create drug libraries. The design of peptide mimetics can be aided by identifying amino acid mutations that increase or decrease binding of IL-9 to its receptor. Approaches that can be used include the yeast two hybrid method (see Chien et al. (1991) Proc. Natl. Acad. Sci. USA 88, 9578-9582) and using the phage display method. The two hybrid method detects protein-protein interactions in yeast (Fields et al. (1989) Nature 340, 245-246). The phage display method detects the interaction between an immobilized protein and a protein that is expressed on the surface of phages such as lambda and M13 (Aniberg et al. (1993) Strategies 6, 2-4; Hogrefe et al. (1993) Gene 128, 119-126). These methods allow positive and negative selection for protein-protein interactions and the identification of the sequences that determine these interactions.

[0087] Without further description, it is believed that one of ordinary skill in the art can, using the preceding description and the following illustrative examples, make and utilize the compounds of the present invention and practice the claimed methods. The following working examples therefore, specifically point out preferred embodiments of the present invention, and are not to be construed as limiting in any way the remainder of the disclosure.

EXAMPLE 1

[0088] IL-13 is Induced In Vivo by IL-9

[0089] Tg5 is a FVB mouse overexpressing the IL-9 gene as previously described (Renauld et al., (1994) Oncogene 9, 1327-1332). To confirm that IL-13 is induced by IL-9 in the lung, RNA from the lungs of TgS and FVB mice was isolated using Trizol as described by the manufacturer (Gibco/BRL). For Northern blot analysis, total RNA derived from Tg5 or FVB lungs was electrophoresed on 1.5% formaldehyde gels, transferred to nylon membranes and probed with a DNA fragment comprising the entire open reading frame of murine IL-13 cDNA. GAPDH was used as an internal control to assess for RNA loading.

[0090] The results of the expression studies demonstrated that IL-13 is specifically expressed in the lung of the IL-9 transgenic mouse but not in the parental strain (FIG. 1). This data demonstrated an effect of IL-9 on IL-13 expression in the lung, where IL-9 responsive cells contained within the lung express IL-13.

EXAMPLE 2

[0091] IL-13 is Induced In Vitro by IL-9

[0092] The murine bone marrow-derived mast cell line L138 and the thymic T-cell lymphoma BW51.47 were cultured in medium containing saturating concentrations of the indicated cytolines as follows: two days in the presence of 100 U/ml rIL-4 or 200 U/ml recombinant IL-9 for BW51.47 cells, two days in the presence of 1 ng/ml of rIL-3 or 200 U/ml rIL-9 for L138 cells.

[0093] Two independent strains of homozygous transgenic mice, designated Tg5 and Tg54, were used in this study. Both strains have circulating IL-9 levels>1 μg/ml, while IL-9 is undetectable in the serum of control FVB mice (Renauld et al. (1994) Oncogene 9, 1327-1332). Total RNA was extracted from the glandular stomach and lungs of six to eight week old Tg5, Tg54, or normal FVB mice (three mice per group).

[0094] Total cellular RNA was isolated from the cytoline treated cell lines or the mouse tissue by the guanidine thiocyanate/CsCl ultra-centrifugation method, and reverse transcription was performed on 10 μg total RNA with an oligo(dT) primer. cDNA corresponding to 100 ng of total RNA was amplified by PCR with the following IL-13 specific primers: sense 5′TGGGTGACTGCAGTCCTGGCT-3′, (SEQ ID NO: 1) antisense 5′GTTGCTTTGTGTAGCTGAGCA-3′. (SEQ ID NO: 2)

[0095] An aliquot of the PCR reaction was run in a 1% agarose gel stained with ethidium bromide.

[0096] As seen in FIG. 2, IL-13 message was seen only in the cell lines treated with IL-9 and not when treated with IL-3 or IL-4. In addition, the IL-13 message was only seen in the tissue of the IL-9 transgenic mice and not in the control mice which have no detectable levels of circulating IL-9. These data clearly indicate that IL-13 is up-regulated by IL-9 and suggest that IL-9 driven up-regulation can be blocked by IL-9 antagonists.

EXAMPLE 3

[0097] Inhibition of Antigen Induced Induction of IL-13 in the Lung with Anti-IL-9

[0098] IL-9 is a major mediator of the asthmatic response in man and mouse models of asthma (Nicolaides et al. (1997) Proc. Natl. Acad. Sci. 94, 13175-13180; McLane et al. (1998) Am. J. Respir. Cell Mol. Biol. 19, 713-720; Temann et al. (1998) J. Exp. Med. 188, 1307-1320; Levitt et al. (1999) Emerg. Thera. Targets 3, 1-11). The use of IL-9 blocking antibodies in antigen exposed mice suppresses the asthmatic-like phenotype (bronchial hyperresponsiveness, mucus overproduction and influx of inflammatory cells such as eosinophils).

[0099] (B6D2)F1 mice were exposed to Aspergillus funagatus antigen intranasally as described (McLane et al. (1998) Am. J. Respir. Cell Mol. Biol. 19, 713-720) on days zero, seven, fourteen, twenty-one and twenty-two. A subset of mice were also treated with 200 μg of anti-mIL-9 (Pharmingen hamster anti-mouse IL-9) or control IgG, by intratracheal instillation on days zero, seven, fourteen and twenty-one. All mice and IgG controls were tested for levels of IL-13 in bronchial lavage fluid using a standard ELISA (R&D Systems). As shown in FIG. 3, anti-IL-9 treatment was able to significantly suppress IL-13 to levels near that of naive. These data show that blocking the function of IL-9 can reduce the elevated levels of IL-13 resulting from exposure to antigen in a murine model of asthma.

EXAMPLE 4

[0100] Effect of Intra-Tracheal Instillation of IL-9 Antibody on IL-13 Gene Expression

[0101] Sixteen, male B6D2F1/J mice (Jackson Laboratories) aged four to five weeks were divided into four treatment groups. Animals in groups one through three each received 50 μl of Aspergillus fumigatus (Holister-Steir) allergenic extract (1:50 w/v in 10% glycerol) intranasaUy on days zero, seven, fourteen, twenty-one and twenty-two. Mice in group four received no treatment as a naive control. For antibody treatments, mice in group two received 200 μg of a control antibody 4, a non-neutralizing anti-murine IL-9 antibody, Genentech), whereas group three received 200 μg of D93 (hamster anti-murine IL-9 antibody with neutralizing activity, Pharmingen). Antibodies were administered intra-tracheally on days zero, seven, fourteen and twenty-one, approximately three hours prior to A. fumigatus exposure. On day twenty-three, approximately sixteen hours after the last A. fumigatus challenge, mice were anesthetized for measurement of airway hyperresponsiveness to intravenous serotonin. Mice in group one, as an infective control, received no antibody but received all challenge doses. Mice were terminally bled for serum immunoglobulin analysis, and broncho-alveolar lavage fluid was collected for cell counts and differentials. Finally, lungs were removed and flash frozen in liquid nitrogen.

[0102] RNA was isolated from frozen lungs using Trizol™ (Invitrogen) according to manufacturer's instructions. Contaminating genomic DNA was removed using the DNA-free kit (Ambion). IL-13 RNA was reverse-transcribed into cDNA using Omniscript™ (Qiagen). cDNA from approximately 125 ng starting RNA was used in each PCR reaction. Real-time PCR reaction was carried out in a 25 μL volume containing 1× Quantitect™ probe master mix (Qiagen), 0.4 μM each of the forward and reverse primers, 0.25 μM of Taqman™ probe, in an ABI PRISM 7700 Sequence Detection System (Applied Biosystems). Primers and probes were designed using Primer Express software. Amplification signals were generated through the cleavage of the 5′ FAM reporter on the Taqman™ probe by the Taq polymerase. Upon cleavage of the probe, the 5′ reporter was removed from the 3′ quencher, resulting in fluorescent signals. The cycle number at which the fluorescent signal crosses an arbitrarily determined threshold is designated C_(T). When the threshold is set in the exponential amplification phase, C_(T) correlates inversely with the log of the starting copy number. To construct a standard curve, RNA from Concavalin A-stimulated murine splenocytes was reverse-transcribed, serially diluted to yield materials for standards. FIG. 4 shows that IL-13 expression is reduced in mice treated with the control anti-IL-9 antibody (w/Af+ctr Ab) versus infective controls (w/Af). However, mice treated with neutralizing anti-IL-9 antibody (w/M+IL-9 Ab) demonstrated a significant decrease in IL-13 expression versus both the infective controls and the control antibody treated mice. One arbitrary unit (A.U.) is equivalent to 1 ng starting RNA from splenocytes. IL-13 and GAPDH mRNA levels for all samples were assayed in duplicates. IL-13 levels were normalized against GAPDH levels for each sample before calculation of the means and standard errors of the means.

[0103] While the invention has been described and illustrated herein by references to various specific materials, procedures and examples, it is understood that the invention is not restricted to the particular combinations of material and procedures selected for that purpose. Numerous variations of such details can be implied as will be appreciated by those skilled in the art. It is intended that the specification and examples be considered as exemplary, only, with the true scope and spirit of the invention being indicated by the following claims. All references, patents and patent applications referred to in this application are herein incorporated by reference in their entirety.

1 18 1 21 DNA Mus musculus 1 tgggtgactg cagtcctggc t 21 2 21 DNA Mus musculus 2 gttgctttgt gtagctgagc a 21 3 591 DNA Homo sapiens CDS (12)..(446) 3 ccgctgtcaa g atg ctt ctg gcc atg gtc ctt acc tct gcc ctg ctc ctg 50 Met Leu Leu Ala Met Val Leu Thr Ser Ala Leu Leu Leu 1 5 10 tgc tcc gtg gca ggc cag ggg tgt cca acc ttg gcg ggg atc ctg gac 98 Cys Ser Val Ala Gly Gln Gly Cys Pro Thr Leu Ala Gly Ile Leu Asp 15 20 25 atc aac ttc ctc atc aac aag atg cag gaa gat cca gct tcc aag tgc 146 Ile Asn Phe Leu Ile Asn Lys Met Gln Glu Asp Pro Ala Ser Lys Cys 30 35 40 45 cac tgc agt gct aat gtg acc agt tgt ctc tgt ttg ggc att ccc tct 194 His Cys Ser Ala Asn Val Thr Ser Cys Leu Cys Leu Gly Ile Pro Ser 50 55 60 gac aac tgc acc aga cca tgc ttc agt gag aga ctg tct cag atg acc 242 Asp Asn Cys Thr Arg Pro Cys Phe Ser Glu Arg Leu Ser Gln Met Thr 65 70 75 aat acc acc atg caa aca aga tac cca ctg att ttc agt cgg gtg aaa 290 Asn Thr Thr Met Gln Thr Arg Tyr Pro Leu Ile Phe Ser Arg Val Lys 80 85 90 aaa tca gtt gaa gta cta aag aac aac aag tgt cca tat ttt tcc tgt 338 Lys Ser Val Glu Val Leu Lys Asn Asn Lys Cys Pro Tyr Phe Ser Cys 95 100 105 gaa cag cca tgc aac caa acc acg gca ggc aac gcg ctg aca ttt ctg 386 Glu Gln Pro Cys Asn Gln Thr Thr Ala Gly Asn Ala Leu Thr Phe Leu 110 115 120 125 aag agt ctt ctg gaa att ttc cag aaa gaa aag atg aga ggg atg aga 434 Lys Ser Leu Leu Glu Ile Phe Gln Lys Glu Lys Met Arg Gly Met Arg 130 135 140 ggc aag ata tga agatgaaata ttatttatcc tatttattaa atttaaaaag 486 Gly Lys Ile ctttctcttt aagttgctac aatttaaaaa tcaagtaagc tactctaaat cagtatcagt 546 tgtgattatt tgtttaacat tgtatgtctt tattttgaaa taaat 591 4 144 PRT Homo sapiens 4 Met Leu Leu Ala Met Val Leu Thr Ser Ala Leu Leu Leu Cys Ser Val 1 5 10 15 Ala Gly Gln Gly Cys Pro Thr Leu Ala Gly Ile Leu Asp Ile Asn Phe 20 25 30 Leu Ile Asn Lys Met Gln Glu Asp Pro Ala Ser Lys Cys His Cys Ser 35 40 45 Ala Asn Val Thr Ser Cys Leu Cys Leu Gly Ile Pro Ser Asp Asn Cys 50 55 60 Thr Arg Pro Cys Phe Ser Glu Arg Leu Ser Gln Met Thr Asn Thr Thr 65 70 75 80 Met Gln Thr Arg Tyr Pro Leu Ile Phe Ser Arg Val Lys Lys Ser Val 85 90 95 Glu Val Leu Lys Asn Asn Lys Cys Pro Tyr Phe Ser Cys Glu Gln Pro 100 105 110 Cys Asn Gln Thr Thr Ala Gly Asn Ala Leu Thr Phe Leu Lys Ser Leu 115 120 125 Leu Glu Ile Phe Gln Lys Glu Lys Met Arg Gly Met Arg Gly Lys Ile 130 135 140 5 1944 DNA Homo sapiens CDS (180)..(1745) 5 agcagctctg taatgcgctt gtggtttcag atgtgggcgg cctgtgtgaa cctgtcgtgc 60 aaagctcacg tcaccaactg ctgcagttat ctcctgaatc aggctgaggg tctttgctgt 120 gcacccagag atagttgggt gacaaatcac ctccaggttg gggatgcctc agacttgtg 179 atg gga ctg ggc aga tgc atc tgg gaa ggc tgg acc ttg gag agt gag 227 Met Gly Leu Gly Arg Cys Ile Trp Glu Gly Trp Thr Leu Glu Ser Glu 1 5 10 15 gcc ctg agg cga gac atg ggc acc tgg ctc ctg gcc tgc atc tgc atc 275 Ala Leu Arg Arg Asp Met Gly Thr Trp Leu Leu Ala Cys Ile Cys Ile 20 25 30 tgc acc tgt gtc tgc ttg gga gtc tct gtc aca ggg gaa gga caa ggg 323 Cys Thr Cys Val Cys Leu Gly Val Ser Val Thr Gly Glu Gly Gln Gly 35 40 45 cca agg tct aga acc ttc acc tgc ctc acc aac aac att ctc agg atc 371 Pro Arg Ser Arg Thr Phe Thr Cys Leu Thr Asn Asn Ile Leu Arg Ile 50 55 60 gat tgc cac tgg tct gcc cca gag ctg gga cag ggc tcc agc ccc tgg 419 Asp Cys His Trp Ser Ala Pro Glu Leu Gly Gln Gly Ser Ser Pro Trp 65 70 75 80 ctc ctc ttc acc agc aac cag gct cct ggc ggc aca cat aag tgc atc 467 Leu Leu Phe Thr Ser Asn Gln Ala Pro Gly Gly Thr His Lys Cys Ile 85 90 95 ttg cgg ggc agt gag tgc acc gtc gtg ctg cca cct gag gca gtg ctc 515 Leu Arg Gly Ser Glu Cys Thr Val Val Leu Pro Pro Glu Ala Val Leu 100 105 110 gtg cca tct gac aat ttc acc atc act ttc cac cac tgc atg tct ggg 563 Val Pro Ser Asp Asn Phe Thr Ile Thr Phe His His Cys Met Ser Gly 115 120 125 agg gag cag gtc agc ctg gtg gac ccg gag tac ctg ccc cgg aga cac 611 Arg Glu Gln Val Ser Leu Val Asp Pro Glu Tyr Leu Pro Arg Arg His 130 135 140 gtt aag ctg gac ccg ccc tct gac ttg cag agc aac atc agt tct ggc 659 Val Lys Leu Asp Pro Pro Ser Asp Leu Gln Ser Asn Ile Ser Ser Gly 145 150 155 160 cac tgc atc ctg acc tgg agc atc agt cct gcc ttg gag cca atg acc 707 His Cys Ile Leu Thr Trp Ser Ile Ser Pro Ala Leu Glu Pro Met Thr 165 170 175 aca ctt ctc agc tat gag ctg gcc ttc aag aag cag gaa gag gcc tgg 755 Thr Leu Leu Ser Tyr Glu Leu Ala Phe Lys Lys Gln Glu Glu Ala Trp 180 185 190 gag cag gcc cag cac agg gat cac att gtc ggg gtg acc tgg ctt ata 803 Glu Gln Ala Gln His Arg Asp His Ile Val Gly Val Thr Trp Leu Ile 195 200 205 ctt gaa gcc ttt gag ctg gac cct ggc ttt atc cat gag gcc agg ctg 851 Leu Glu Ala Phe Glu Leu Asp Pro Gly Phe Ile His Glu Ala Arg Leu 210 215 220 cgt gtc cag atg gcc aca ctg gag gat gat gtg gta gag gag gag cgt 899 Arg Val Gln Met Ala Thr Leu Glu Asp Asp Val Val Glu Glu Glu Arg 225 230 235 240 tat aca ggc cag tgg agt gag tgg agc cag cct gtg tgc ttc cag gct 947 Tyr Thr Gly Gln Trp Ser Glu Trp Ser Gln Pro Val Cys Phe Gln Ala 245 250 255 ccc cag aga caa ggc cct ctg atc cca ccc tgg ggg tgg cca ggc aac 995 Pro Gln Arg Gln Gly Pro Leu Ile Pro Pro Trp Gly Trp Pro Gly Asn 260 265 270 acc ctt gtt gct gtg tcc atc ttt ctc ctg ctg act ggc ccg acc tac 1043 Thr Leu Val Ala Val Ser Ile Phe Leu Leu Leu Thr Gly Pro Thr Tyr 275 280 285 ctc ctg ttc aag ctg tcg ccc agg gtg aag aga atc ttc tac cag aac 1091 Leu Leu Phe Lys Leu Ser Pro Arg Val Lys Arg Ile Phe Tyr Gln Asn 290 295 300 gtg ccc tct cca gcg atg ttc ttc cag ccc ctc tac agt gta cac aat 1139 Val Pro Ser Pro Ala Met Phe Phe Gln Pro Leu Tyr Ser Val His Asn 305 310 315 320 ggg aac ttc cag act tgg atg ggg gcc cac ggg gcc ggt gtg ctg ttg 1187 Gly Asn Phe Gln Thr Trp Met Gly Ala His Gly Ala Gly Val Leu Leu 325 330 335 agc cag gac tgt gct ggc acc cca cag gga gcc ttg gag ccc tgc gtc 1235 Ser Gln Asp Cys Ala Gly Thr Pro Gln Gly Ala Leu Glu Pro Cys Val 340 345 350 cag gag gcc act gca ctg ctc act tgt ggc cca gcg cgt cct tgg aaa 1283 Gln Glu Ala Thr Ala Leu Leu Thr Cys Gly Pro Ala Arg Pro Trp Lys 355 360 365 tct gtg gcc ctg gag gag gaa cag gag ggc cct ggg acc agg ctc ccg 1331 Ser Val Ala Leu Glu Glu Glu Gln Glu Gly Pro Gly Thr Arg Leu Pro 370 375 380 ggg aac ctg agc tca gag gat gtg ctg cca gca ggg tgt acg gag tgg 1379 Gly Asn Leu Ser Ser Glu Asp Val Leu Pro Ala Gly Cys Thr Glu Trp 385 390 395 400 agg gta cag acg ctt gcc tat ctg cca cag gag gac tgg gcc ccc acg 1427 Arg Val Gln Thr Leu Ala Tyr Leu Pro Gln Glu Asp Trp Ala Pro Thr 405 410 415 tcc ctg act agg ccg gct ccc cca gac tca gag ggc agc agg agc agc 1475 Ser Leu Thr Arg Pro Ala Pro Pro Asp Ser Glu Gly Ser Arg Ser Ser 420 425 430 agc agc agc agc agc agc aac aac aac aac tac tgt gcc ttg ggc tgc 1523 Ser Ser Ser Ser Ser Ser Asn Asn Asn Asn Tyr Cys Ala Leu Gly Cys 435 440 445 tat ggg gga tgg cac ctc tca gcc ctc cca gga aac aca cag agc tct 1571 Tyr Gly Gly Trp His Leu Ser Ala Leu Pro Gly Asn Thr Gln Ser Ser 450 455 460 ggg ccc atc cca gcc ctg gcc tgt ggc ctt tct tgt gac cat cag ggc 1619 Gly Pro Ile Pro Ala Leu Ala Cys Gly Leu Ser Cys Asp His Gln Gly 465 470 475 480 ctg gag acc cag caa gga gtt gcc tgg gtg ctg gct ggt cac tgc cag 1667 Leu Glu Thr Gln Gln Gly Val Ala Trp Val Leu Ala Gly His Cys Gln 485 490 495 agg cct ggg ctg cat gag gac ctc cag ggc atg ttg ctc cct tct gtc 1715 Arg Pro Gly Leu His Glu Asp Leu Gln Gly Met Leu Leu Pro Ser Val 500 505 510 ctc agc aag gct cgg tcc tgg aca ttc tag gtccctgact cgccagatgc 1765 Leu Ser Lys Ala Arg Ser Trp Thr Phe 515 520 atcatgtcca ttttgggaaa atggactgaa gtttctggag cccttgtctg agactgaacc 1825 tcctgagaag gggcccctag cagcggtcag aggtcctgtc tggatggagg ctggaggctc 1885 ccccctcaac ccctctgctc agtgcctgtg gggagcagcc tctaccctca gcatcctgg 1944 6 521 PRT Homo sapiens 6 7 536 DNA Mus musculus CDS (16)..(450) 7 cagactcccg tcaac atg ttg gtg aca tac atc ctt gcc tct gtt ttg ctc 51 Met Leu Val Thr Tyr Ile Leu Ala Ser Val Leu Leu 1 5 10 ttc agt tct gtg ctg ggc cag aga tgc agc acc aca tgg ggc atc aga 99 Phe Ser Ser Val Leu Gly Gln Arg Cys Ser Thr Thr Trp Gly Ile Arg 15 20 25 gac acc aat tac ctt att gaa aat ctg aag gat gat cca ccg tca aaa 147 Asp Thr Asn Tyr Leu Ile Glu Asn Leu Lys Asp Asp Pro Pro Ser Lys 30 35 40 tgc agc tgc agc ggc aac gtg acc agc tgc ttg tgt ctc tcc gtc cca 195 Cys Ser Cys Ser Gly Asn Val Thr Ser Cys Leu Cys Leu Ser Val Pro 45 50 55 60 act gat gat tgt acc aca ccg tgc tac agg gag gga ctg tta cag ctg 243 Thr Asp Asp Cys Thr Thr Pro Cys Tyr Arg Glu Gly Leu Leu Gln Leu 65 70 75 acc aat gcc aca cag aaa tca aga ctc ttg cct gtt ttc cat cgg gtg 291 Thr Asn Ala Thr Gln Lys Ser Arg Leu Leu Pro Val Phe His Arg Val 80 85 90 aaa agg ata gtt gaa gtc cta aag aac atc acg tgt ccg tcc ttt tcc 339 Lys Arg Ile Val Glu Val Leu Lys Asn Ile Thr Cys Pro Ser Phe Ser 95 100 105 tgc gaa aag cca tgc aac cag acc atg gca ggc aac aca ctg tca ttt 387 Cys Glu Lys Pro Cys Asn Gln Thr Met Ala Gly Asn Thr Leu Ser Phe 110 115 120 ctg aag agt ctc ctg ggg acg ttc cag aag aca gag atg caa agg cag 435 Leu Lys Ser Leu Leu Gly Thr Phe Gln Lys Thr Glu Met Gln Arg Gln 125 130 135 140 aaa agc cga cca tga agacagatgc tatttattct atttattgaa tttacaaaac 490 Lys Ser Arg Pro ctcccctcct taactgttac agtgaagaaa taaactaagc tattct 536 8 144 PRT Mus musculus 8 Met Leu Val Thr Tyr Ile Leu Ala Ser Val Leu Leu Phe Ser Ser Val 1 5 10 15 Leu Gly Gln Arg Cys Ser Thr Thr Trp Gly Ile Arg Asp Thr Asn Tyr 20 25 30 Leu Ile Glu Asn Leu Lys Asp Asp Pro Pro Ser Lys Cys Ser Cys Ser 35 40 45 Gly Asn Val Thr Ser Cys Leu Cys Leu Ser Val Pro Thr Asp Asp Cys 50 55 60 Thr Thr Pro Cys Tyr Arg Glu Gly Leu Leu Gln Leu Thr Asn Ala Thr 65 70 75 80 Gln Lys Ser Arg Leu Leu Pro Val Phe His Arg Val Lys Arg Ile Val 85 90 95 Glu Val Leu Lys Asn Ile Thr Cys Pro Ser Phe Ser Cys Glu Lys Pro 100 105 110 Cys Asn Gln Thr Met Ala Gly Asn Thr Leu Ser Phe Leu Lys Ser Leu 115 120 125 Leu Gly Thr Phe Gln Lys Thr Glu Met Gln Arg Gln Lys Ser Arg Pro 130 135 140 9 3026 DNA Mus musculus CDS (5)..(1411) 9 ctcc atg gcc ctg gga aga tgc att gcg gaa ggt tgg acc ttg gag aga 49 Met Ala Leu Gly Arg Cys Ile Ala Glu Gly Trp Thr Leu Glu Arg 1 5 10 15 gtg gcg gtg aaa cag gtc tcc tgg ttc ctg atc tac agc tgg gtc tgc 97 Val Ala Val Lys Gln Val Ser Trp Phe Leu Ile Tyr Ser Trp Val Cys 20 25 30 tct gga gtc tgc cgg gga gtc tcg gtc cca gag caa gga gga gga ggg 145 Ser Gly Val Cys Arg Gly Val Ser Val Pro Glu Gln Gly Gly Gly Gly 35 40 45 cag aag gct gga gca ttc acc tgt ctc agc aac agt att tac agg atc 193 Gln Lys Ala Gly Ala Phe Thr Cys Leu Ser Asn Ser Ile Tyr Arg Ile 50 55 60 gac tgc cac tgg tcg gct cca gag ctg ggc cag gaa tcc agg gcc tgg 241 Asp Cys His Trp Ser Ala Pro Glu Leu Gly Gln Glu Ser Arg Ala Trp 65 70 75 ctc ctc ttt acc agt aac cag gtg act gaa atc aaa cac aaa tgc acc 289 Leu Leu Phe Thr Ser Asn Gln Val Thr Glu Ile Lys His Lys Cys Thr 80 85 90 95 ttc tgg gac agt atg tgt acc ctg gtg ctg cct aaa gag gag gtg ttc 337 Phe Trp Asp Ser Met Cys Thr Leu Val Leu Pro Lys Glu Glu Val Phe 100 105 110 tta cct ttt gac aac ttc acc atc aca ctt cac cgc tgc atc atg gga 385 Leu Pro Phe Asp Asn Phe Thr Ile Thr Leu His Arg Cys Ile Met Gly 115 120 125 cag gaa cag gtc agc ctg gtg gac tca cag tac ctg ccc agg aga cac 433 Gln Glu Gln Val Ser Leu Val Asp Ser Gln Tyr Leu Pro Arg Arg His 130 135 140 atc aag ttg gac cca ccc tct gat ctg cag agc aat gtc agc tct ggg 481 Ile Lys Leu Asp Pro Pro Ser Asp Leu Gln Ser Asn Val Ser Ser Gly 145 150 155 cgt tgt gtc ctg acc tgg ggt atc aat ctt gcc ctg gag cca ttg atc 529 Arg Cys Val Leu Thr Trp Gly Ile Asn Leu Ala Leu Glu Pro Leu Ile 160 165 170 175 aca tcc ctc agc tac gag ctg gcc ttc aag agg cag gaa gag gcc tgg 577 Thr Ser Leu Ser Tyr Glu Leu Ala Phe Lys Arg Gln Glu Glu Ala Trp 180 185 190 gag gcc cgg cac aag gac cgt atc gtt gga gtg acc tgg ctc atc ctt 625 Glu Ala Arg His Lys Asp Arg Ile Val Gly Val Thr Trp Leu Ile Leu 195 200 205 gaa gcc gtc gaa ctg aat cct ggt tcc atc tac gag gcc agg ctg cgt 673 Glu Ala Val Glu Leu Asn Pro Gly Ser Ile Tyr Glu Ala Arg Leu Arg 210 215 220 gtc cag atg act ttg gag agt tat gag gac aag aca gag ggg gaa tat 721 Val Gln Met Thr Leu Glu Ser Tyr Glu Asp Lys Thr Glu Gly Glu Tyr 225 230 235 tat aag agc cat tgg agt gag tgg agc cag ccc gtg tcc ttt cct tct 769 Tyr Lys Ser His Trp Ser Glu Trp Ser Gln Pro Val Ser Phe Pro Ser 240 245 250 255 ccc cag agg aga cag ggc ctc ctg gtc cca cgc tgg caa tgg tca gcc 817 Pro Gln Arg Arg Gln Gly Leu Leu Val Pro Arg Trp Gln Trp Ser Ala 260 265 270 agc atc ctt gta gtt gtg ccc atc ttt ctt ctg ctg act ggc ttt gtc 865 Ser Ile Leu Val Val Val Pro Ile Phe Leu Leu Leu Thr Gly Phe Val 275 280 285 cac ctt ctg ttc aag ctg tca ccc agg ctg aag aga atc ttt tac cag 913 His Leu Leu Phe Lys Leu Ser Pro Arg Leu Lys Arg Ile Phe Tyr Gln 290 295 300 aac att cca tct ccc gag gcg ttc ttc cat cct ctc tac agt gtg tac 961 Asn Ile Pro Ser Pro Glu Ala Phe Phe His Pro Leu Tyr Ser Val Tyr 305 310 315 cat ggg gac ttc cag agt tgg aca ggg gcc cgc aga gcc gga cca caa 1009 His Gly Asp Phe Gln Ser Trp Thr Gly Ala Arg Arg Ala Gly Pro Gln 320 325 330 335 gca aga cag aat ggt gtc agt act tca tca gca ggc tca gag tcc agc 1057 Ala Arg Gln Asn Gly Val Ser Thr Ser Ser Ala Gly Ser Glu Ser Ser 340 345 350 atc tgg gag gcc gtc gcc aca ctc acc tat agc ccg gca tgc cct gtg 1105 Ile Trp Glu Ala Val Ala Thr Leu Thr Tyr Ser Pro Ala Cys Pro Val 355 360 365 cag ttt gcc tgc ctg aag tgg gag gcc aca gcc ccg ggc ttc cca ggg 1153 Gln Phe Ala Cys Leu Lys Trp Glu Ala Thr Ala Pro Gly Phe Pro Gly 370 375 380 ctc cca ggc tca gag cat gtg ctg ccg gca ggg tgt ctg gag ttg gaa 1201 Leu Pro Gly Ser Glu His Val Leu Pro Ala Gly Cys Leu Glu Leu Glu 385 390 395 gga cag cca tct gcc tac ctg ccc cag gag gac tgg gcc cca ctg ggc 1249 Gly Gln Pro Ser Ala Tyr Leu Pro Gln Glu Asp Trp Ala Pro Leu Gly 400 405 410 415 tct gcc agg ccc cct cct cca gac tca gac agc ggc agc agc gac tat 1297 Ser Ala Arg Pro Pro Pro Pro Asp Ser Asp Ser Gly Ser Ser Asp Tyr 420 425 430 tgc atg ttg gac tgc tgt gag gaa tgc cac ctc tca gcc ttc cca gga 1345 Cys Met Leu Asp Cys Cys Glu Glu Cys His Leu Ser Ala Phe Pro Gly 435 440 445 cac acc gag agt cct gag ctc acg cta gct cag cct gtg gcc ctt cct 1393 His Thr Glu Ser Pro Glu Leu Thr Leu Ala Gln Pro Val Ala Leu Pro 450 455 460 gtg tcc agc agg gcc tga cacctaccaa gggatgtggg cattctcttc 1441 Val Ser Ser Arg Ala 465 cctcctatcc tcggatggca ccagacacag tctctgcgtg tctctgctag gtgcaccatg 1501 tctgttttgg ggagatgaac gaaaggcccc aggctgaccc tggggtgcgt gtggaactcc 1561 ggagaggagg cagctgtgca cggatcagag gcaatgcgga tggaagcagt agactgtgcc 1621 ttacccccct gctctgcctt tgtggtgggg atgcctccag ggtcagcatc ttaacatccg 1681 ccttcgcttc tcttgtcttt ctggctctgt cccaggcctg aaaaaagaat gtgacaagca 1741 gcctggtctg ttcttccacc cctaaagggc tggcctgggc ccagggacac tgatgagaca 1801 acattggtga agtgtccctt ttcagtgcct ttcccattaa gaccagaagg gacgcttttg 1861 actgcaggct gtgggtggct gggtacggag ggaatgatgg agctttgagc aggtggggtt 1921 gtccatcttt gagcttttgg ggttccaaga tcagctggaa ggagtctcac cgactgattc 1981 aaagaagtct tacccatctg tgatattttc tttcctggtg ccgtgataaa acaccgtgac 2041 caaaaatgac ttacaaaagg aagagttggc ttggtttaag gttccagagg tgtggagaca 2101 tggcagccag cggcacacat ggcagtgagg acaggaagct gagagctcac atctcaacca 2161 aaagttgagt gaactgaaag tactatcccc tcccccaccc caactccagc aaggctccac 2221 ccccctgaag gttccatgcc tccctaaaca gctcggccaa atagagacca agtgttcaaa 2281 tatctgagtc tgtgggggac atttctcatt caaaccactt cactgccccc actgttccta 2341 ggaaaaagct gaagccaggg ctactggaca gggttgggaa tggctatttc tcagcagccg 2401 gcctgtgaag aatgacgatg cccctaactg ccttctgagg tagcctggag agagctgtgg 2461 gtgggctaga atgtggctgt tattttccta ggcttgccct aacagaatac cagaaaccgg 2521 gtggctaata ccgtagattt gttttctctc tgctctgagg tccatgggtc tggaatggag 2581 acaccaggaa ggccatgctc ctggagggaa gggtttgttt ccagccctgc ttcacattcc 2641 cctctgagtg tcctcttgcg tactgagact agatgctacc caatgacggg gacaggttgt 2701 gtctcatact cttgcatgtg agcagagatt gtgacctaga aggccaaaac aggctgagca 2761 gttggccacg tttgtgcaga tttggagcca taaagcactg gcctaacaga agtcctcttg 2821 ctccttgaag ggctcttaaa gggcaagcgt gggaacaatg ctagtgtgag gactatttcc 2881 aagcctgtga caccgtgcaa gagacggtcg aactactgcg cagggtccat ggagcgcaga 2941 gtccatggag cgcagagagg aactgcatgc agcattgtga gctcagagct ggtgtcctgg 3001 gaaggctcac aatgctgacc ccagg 3026 10 468 PRT Mus musculus 10 Met Ala Leu Gly Arg Cys Ile Ala Glu Gly Trp Thr Leu Glu Arg Val 1 5 10 15 Ala Val Lys Gln Val Ser Trp Phe Leu Ile Tyr Ser Trp Val Cys Ser 20 25 30 Gly Val Cys Arg Gly Val Ser Val Pro Glu Gln Gly Gly Gly Gly Gln 35 40 45 Lys Ala Gly Ala Phe Thr Cys Leu Ser Asn Ser Ile Tyr Arg Ile Asp 50 55 60 Cys His Trp Ser Ala Pro Glu Leu Gly Gln Glu Ser Arg Ala Trp Leu 65 70 75 80 Leu Phe Thr Ser Asn Gln Val Thr Glu Ile Lys His Lys Cys Thr Phe 85 90 95 Trp Asp Ser Met Cys Thr Leu Val Leu Pro Lys Glu Glu Val Phe Leu 100 105 110 Pro Phe Asp Asn Phe Thr Ile Thr Leu His Arg Cys Ile Met Gly Gln 115 120 125 Glu Gln Val Ser Leu Val Asp Ser Gln Tyr Leu Pro Arg Arg His Ile 130 135 140 Lys Leu Asp Pro Pro Ser Asp Leu Gln Ser Asn Val Ser Ser Gly Arg 145 150 155 160 Cys Val Leu Thr Trp Gly Ile Asn Leu Ala Leu Glu Pro Leu Ile Thr 165 170 175 Ser Leu Ser Tyr Glu Leu Ala Phe Lys Arg Gln Glu Glu Ala Trp Glu 180 185 190 Ala Arg His Lys Asp Arg Ile Val Gly Val Thr Trp Leu Ile Leu Glu 195 200 205 Ala Val Glu Leu Asn Pro Gly Ser Ile Tyr Glu Ala Arg Leu Arg Val 210 215 220 Gln Met Thr Leu Glu Ser Tyr Glu Asp Lys Thr Glu Gly Glu Tyr Tyr 225 230 235 240 Lys Ser His Trp Ser Glu Trp Ser Gln Pro Val Ser Phe Pro Ser Pro 245 250 255 Gln Arg Arg Gln Gly Leu Leu Val Pro Arg Trp Gln Trp Ser Ala Ser 260 265 270 Ile Leu Val Val Val Pro Ile Phe Leu Leu Leu Thr Gly Phe Val His 275 280 285 Leu Leu Phe Lys Leu Ser Pro Arg Leu Lys Arg Ile Phe Tyr Gln Asn 290 295 300 Ile Pro Ser Pro Glu Ala Phe Phe His Pro Leu Tyr Ser Val Tyr His 305 310 315 320 Gly Asp Phe Gln Ser Trp Thr Gly Ala Arg Arg Ala Gly Pro Gln Ala 325 330 335 Arg Gln Asn Gly Val Ser Thr Ser Ser Ala Gly Ser Glu Ser Ser Ile 340 345 350 Trp Glu Ala Val Ala Thr Leu Thr Tyr Ser Pro Ala Cys Pro Val Gln 355 360 365 Phe Ala Cys Leu Lys Trp Glu Ala Thr Ala Pro Gly Phe Pro Gly Leu 370 375 380 Pro Gly Ser Glu His Val Leu Pro Ala Gly Cys Leu Glu Leu Glu Gly 385 390 395 400 Gln Pro Ser Ala Tyr Leu Pro Gln Glu Asp Trp Ala Pro Leu Gly Ser 405 410 415 Ala Arg Pro Pro Pro Pro Asp Ser Asp Ser Gly Ser Ser Asp Tyr Cys 420 425 430 Met Leu Asp Cys Cys Glu Glu Cys His Leu Ser Ala Phe Pro Gly His 435 440 445 Thr Glu Ser Pro Glu Leu Thr Leu Ala Gln Pro Val Ala Leu Pro Val 450 455 460 Ser Ser Arg Ala 465 11 1283 DNA Homo sapiens CDS (57)..(455) 11 aagccaccca gcctatgcat ccgctcctca atcctctcct gttggcactg ggcctc atg 59 Met 1 gcg ctt ttg ttg acc acg gtc att gct ctc act tgc ctt ggc ggc ttt 107 Ala Leu Leu Leu Thr Thr Val Ile Ala Leu Thr Cys Leu Gly Gly Phe 5 10 15 gcc tcc cca ggc cct gtg cct ccc tct aca gcc ctc agg gag ctc att 155 Ala Ser Pro Gly Pro Val Pro Pro Ser Thr Ala Leu Arg Glu Leu Ile 20 25 30 gag gag ctg gtc aac atc acc cag aac cag aag gct ccg ctc tgc aat 203 Glu Glu Leu Val Asn Ile Thr Gln Asn Gln Lys Ala Pro Leu Cys Asn 35 40 45 ggc agc atg gta tgg agc atc aac ctg aca gct ggc atg tac tgt gca 251 Gly Ser Met Val Trp Ser Ile Asn Leu Thr Ala Gly Met Tyr Cys Ala 50 55 60 65 gcc ctg gaa tcc ctg atc aac gtg tca ggc tgc agt gcc atc gag aag 299 Ala Leu Glu Ser Leu Ile Asn Val Ser Gly Cys Ser Ala Ile Glu Lys 70 75 80 acc cag agg atg ctg agc gga ttc tgc ccg cac aag gtc tca gct ggg 347 Thr Gln Arg Met Leu Ser Gly Phe Cys Pro His Lys Val Ser Ala Gly 85 90 95 cag ttt tcc agc ttg cat gtc cga gac acc aaa atc gag gtg gcc cag 395 Gln Phe Ser Ser Leu His Val Arg Asp Thr Lys Ile Glu Val Ala Gln 100 105 110 ttt gta aag gac ctg ctc tta cat tta aag aaa ctt ttt cgc gag gga 443 Phe Val Lys Asp Leu Leu Leu His Leu Lys Lys Leu Phe Arg Glu Gly 115 120 125 cag ttc aac tga aacttcgaaa gcatcattat ttgcagagac aggacctgac 495 Gln Phe Asn 130 tattgaagtt gcagattcat ttttctttct gatgtcaaaa atgtcttggg taggcgggaa 555 ggagggttag ggaggggtaa aattccttag cttagacctc agcctgtgct gcccgtcttc 615 agcctagccg acctcagcct tccccttgcc cagggctcag cctggtgggc ctcctctgtc 675 cagggccctg agctcggtgg acccagggat gacatgtccc tacacccctc ccctgcccta 735 gagcacactg tagcattaca gtgggtgccc cccttgccag acatgtggtg ggacagggac 795 ccacttcaca cacaggcaac tgaggcagac agcagctcag gcacacttct tcttggtctt 855 atttattatt gtgtgttatt taaatgagtg tgtttgtcac cgttggggat tggggaagac 915 tgtggctgct agcacttgga gccaagggtt cagagactca gggccccagc actaaagcag 975 tggacaccag gagtccctgg taataagtac tgtgtacaga attctgctac ctcactgggg 1035 tcctggggcc tcggagcctc atccgaggca gggtcaggag aggggcagaa cagccgctcc 1095 tgtctgccag ccagcagcca gctctcagcc aacgagtaat ttattgtttt tccttgtatt 1155 taaatattaa atatgttagc aaagagttaa tatatagaag ggtaccttga acactggggg 1215 aggggacatt gaacaagttg tttcattgac tatcaaactg aagccagaaa taaagttggt 1275 gacagata 1283 12 132 PRT Homo sapiens 12 Met Ala Leu Leu Leu Thr Thr Val Ile Ala Leu Thr Cys Leu Gly Gly 1 5 10 15 Phe Ala Ser Pro Gly Pro Val Pro Pro Ser Thr Ala Leu Arg Glu Leu 20 25 30 Ile Glu Glu Leu Val Asn Ile Thr Gln Asn Gln Lys Ala Pro Leu Cys 35 40 45 Asn Gly Ser Met Val Trp Ser Ile Asn Leu Thr Ala Gly Met Tyr Cys 50 55 60 Ala Ala Leu Glu Ser Leu Ile Asn Val Ser Gly Cys Ser Ala Ile Glu 65 70 75 80 Lys Thr Gln Arg Met Leu Ser Gly Phe Cys Pro His Lys Val Ser Ala 85 90 95 Gly Gln Phe Ser Ser Leu His Val Arg Asp Thr Lys Ile Glu Val Ala 100 105 110 Gln Phe Val Lys Asp Leu Leu Leu His Leu Lys Lys Leu Phe Arg Glu 115 120 125 Gly Gln Phe Asn 130 13 1207 DNA Mus musculus CDS (70)..(465) 13 gacaagccag cagcctaggc cagcccacag ttctacagct ccctggttct ctcactggct 60 ctgggcttc atg gcg ctc tgg gtg act gca gtc ctg gct ctt gct tgc ctt 111 Met Ala Leu Trp Val Thr Ala Val Leu Ala Leu Ala Cys Leu 1 5 10 ggt ggt ctc gcc gcc cca ggg ccg gtg cca aga tct gtg tct ctc cct 159 Gly Gly Leu Ala Ala Pro Gly Pro Val Pro Arg Ser Val Ser Leu Pro 15 20 25 30 ctg acc ctt aag gag ctt att gag gag ctg agc aac atc aca caa gac 207 Leu Thr Leu Lys Glu Leu Ile Glu Glu Leu Ser Asn Ile Thr Gln Asp 35 40 45 cag act ccc ctg tgc aac ggc agc atg gta tgg agt gtg gac ctg gcc 255 Gln Thr Pro Leu Cys Asn Gly Ser Met Val Trp Ser Val Asp Leu Ala 50 55 60 gct ggc ggg ttc tgt gta gcc ctg gat tcc ctg acc aac atc tcc aat 303 Ala Gly Gly Phe Cys Val Ala Leu Asp Ser Leu Thr Asn Ile Ser Asn 65 70 75 tgc aat gcc atc tac agg acc cag agg ata ttg cat ggc ctc tgt aac 351 Cys Asn Ala Ile Tyr Arg Thr Gln Arg Ile Leu His Gly Leu Cys Asn 80 85 90 cgc aag gcc ccc act acg gtc tcc agc ctc ccc gat acc aaa atc gaa 399 Arg Lys Ala Pro Thr Thr Val Ser Ser Leu Pro Asp Thr Lys Ile Glu 95 100 105 110 gta gcc cac ttt ata aca aaa ctg ctc agc tac aca aag caa ctg ttt 447 Val Ala His Phe Ile Thr Lys Leu Leu Ser Tyr Thr Lys Gln Leu Phe 115 120 125 cgc cac ggc ccc ttc taa tgaggagaga ccatccctgg gcatctcagc 495 Arg His Gly Pro Phe 130 tgtggactca ttttcctttc tcacatcaga ctttgctggg gagaggcagg gaggagggtt 555 gaggaggaag ggagatgcct cagctttggc ctcagcctgc actgcctgcc tagtgctcag 615 ggtctcagcc tggcaacacc cccaccccac ccccaccccc gccgccccat cccatcccta 675 cagaaaactg cagcaagacc gtgagtccag cctgtggcct ggtccacaca gggcaactga 735 ggcaggcagc agcttgagca catttcttct tgatcttatt tattatggtt gtgtgttatt 795 taaatgagtc tgtcagtatc ccggtgggga catggtttgc tgcctatgcc ctgggggctc 855 cagcattgaa gcagtgggct ctggggtccc tggcaatatt actgtataca taactctgct 915 acctcactgt agcctccagg tctcacccca ggcagggaga tgggagggga ggccagagca 975 acactcctgt ctgccacggc agcaaccagc cctcagccat gaaataactt attgttttgt 1035 tcttatattt aaagtattaa atagcttagc aaagagttaa taatatatgg aagaatggcc 1095 tgttacactc aaggtgatgt gtagtgaatg gggggagggt ggtgggtttg tcactgaaca 1155 aacttttcat tgactgtcaa actagaaacc ggaaataaag atggtgacag at 1207 14 131 PRT Mus musculus 14 Met Ala Leu Trp Val Thr Ala Val Leu Ala Leu Ala Cys Leu Gly Gly 1 5 10 15 Leu Ala Ala Pro Gly Pro Val Pro Arg Ser Val Ser Leu Pro Leu Thr 20 25 30 Leu Lys Glu Leu Ile Glu Glu Leu Ser Asn Ile Thr Gln Asp Gln Thr 35 40 45 Pro Leu Cys Asn Gly Ser Met Val Trp Ser Val Asp Leu Ala Ala Gly 50 55 60 Gly Phe Cys Val Ala Leu Asp Ser Leu Thr Asn Ile Ser Asn Cys Asn 65 70 75 80 Ala Ile Tyr Arg Thr Gln Arg Ile Leu His Gly Leu Cys Asn Arg Lys 85 90 95 Ala Pro Thr Thr Val Ser Ser Leu Pro Asp Thr Lys Ile Glu Val Ala 100 105 110 His Phe Ile Thr Lys Leu Leu Ser Tyr Thr Lys Gln Leu Phe Arg His 115 120 125 Gly Pro Phe 130 15 18 PRT Artificial MISC_FEATURE Peptide sequence 15 Ser Asp Asn Ala Thr Arg Pro Ala Phe Ser Glu Arg Leu Ser Gln Met 1 5 10 15 Thr Asn 16 18 PRT Artificial MISC_FEATURE Peptide sequence 16 Phe Ser Arg Val Lys Lys Ser Val Glu Val Leu Lys Asn Asn Lys Ala 1 5 10 15 Pro Tyr 17 18 PRT Artificial MISC_FEATURE Peptide sequence 17 Glu Gln Pro Ala Asn Gln Thr Thr Ala Gly Asn Ala Leu Thr Phe Leu 1 5 10 15 Lys Ser 18 18 PRT Artificial MISC_FEATURE Peptide sequence 18 Thr Ala Gly Asn Ala Leu Thr Phe Leu Lys Ser Leu Leu Glu Ile Phe 1 5 10 15 Gln Lys 

We claim:
 1. A method for modulating IL-13 expression and/or activity in a mammal comprising administering an effective amount of an agent which modulates the expression and/or activity of IL-9.
 2. A method according to claim 1, wherein the IL-13 expression and/or activity is down-regulated.
 3. A method according to claim 2, wherein the agent is an IL-9 anagonist.
 4. A method according to claim 3, wherein the IL-9 antagonist is an antibody against IL-9 or the IL-9 receptor.
 5. A method according to claim 4, wherein the antibody is a monoclonal antibody.
 6. A method according to claim 4, wherein the antibody is a chimeric antibody.
 7. A method according to claim 4, wherein the antibody is a humanized antibody.
 8. A method according to claim 3, wherein the IL-9 antagonist is a soluble IL-9 receptor protein.
 9. A method according to claim 2, wherein the down-regulation of IL-13 alleviates at least one symptom associated with an atopic allergy.
 10. A method according to claim 9, wherein the atopic allergy is asthma.
 11. A method according to claim 10, wherein the at least one symptom associated with asthma is selected from the group consisting of bronchial hyperresponsiveness, bronchoconstriction, bronchial inflammation, pulmonary fibrosis, eosinophilia, elevated serum IgE levels and mucin overproduction.
 12. A method according to claim 2, wherein the down-regulation of IL-13 produces a down-regulation in 15-lipoxygenase expression and/or activity.
 13. A method according to claim 2, wherein the down-regulation of IL-13 produces an up-regulation in isozyme 5-lipoxygenase.expression and/or activity.
 14. A method according to claim 1, wherein the mammal is a human.
 15. A method according to claim 1, wherein the agent is administered by a route selected from the group consisting of intravenous, subcutaneous, transdermal, mucosal, intranasal, oral, bronchial adminstration.
 16. A method according to claim 15, wherein the bronchial administration is carried out with an aerosol inhaler.
 17. A method for the treating a disease associated with elevated levels of IL-13 in a mammal comprising administration of an effective amount of an IL-9 antagonist.
 18. A method according to claim 17, wherein the disease is further associated with a Th1-type inflammatory response.
 19. A method according to claim 17, wherein the IL-9 antagonist is an antibody against IL-9 or the IL-9 receptor.
 20. A method according to claim 19, wherein the antibody is a monoclonal antibody.
 21. A method according to claim 19, wherein the antibody is a chimeric antibody.
 22. A method according to claim 19, wherein the antibody is a humanized antibody.
 23. A method according to claim 17, wherein the IL-9 antagonist is a soluble IL-9 receptor protein.
 24. A method according to claim 17, wherein the disease is an atopic allergy.
 25. A method according to claim 24, wherein the atopic allergy is asthma.
 26. A method according to claim 17, wherein the disease is an infectious disease.
 27. A method according to claim 17, wherein the agent is administered by a route selected from the group consisting of intravenous, subcutaneous, transdermal, mucosal, intranasal, oral, bronchial administration.
 28. A method according to claim 27, wherein the bronchial administration is carried out with an aerosol inhaler.
 29. A method of identifying an agent which modulates IL-13 expression and/or activity comprising: (a) contacting a cell expressing an IL-9 receptor with the agent in the presence of an IL-9 receptor ligand; (b) measuring expression and/or activity of IL-13; wherein a decrease in IL-13 expression and/or activity indicates an agent capable of modulating IL-13 expression and/or activity.
 30. The method of claim 29 wherein said IL-9 receptor ligand is selected from the group consisting of IL-9 or a fragment thereof, an IL-9 analog and an IL-9 peptide mimetic. 